A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3. (Q50448797)

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scientific article published on 22 November 2008

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English	A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3.	scientific article published on 22 November 2008

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instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

title

A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

main subject

hearing loss

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based on heuristic

inferred from title

author name string

Arunima Chatterjee

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1

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Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

Rajeev Jalvi

series ordinal

2

1 reference

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Europe PubMed Central

PubMed publication ID

19030898

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14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

Nishtha Pandey

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3

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Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

R Rangasayee

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4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

Anuranjan Anand

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5

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Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

publication date

22 November 2008

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Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

published in

Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

volume

124

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stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

issue

6

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stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

page(s)

669-675

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stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

cites work

Parametric and nonparametric linkage analysis: a unified multipoint approach

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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Strategies for multilocus linkage analysis in humans

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Autosomal recessive nonsyndromic deafness locus DFNB63 at chromosome 11q13.2-q13.3.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qter.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Genetic epidemiology of hearing impairment

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

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inferred from PubMed ID database lookup

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tricellulin is a tight-junction protein necessary for hearing

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 1993-94 Généthon human genetic linkage map

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

Human Nonsyndromic Sensorineural Deafness

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/19030898

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12 December 2020

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inferred from PubMed ID database lookup

A new locus for nonsyndromic deafness DFNB51 maps to chromosome 11p13-p12.

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Contribution of the N-acetyltransferase 2 polymorphism NAT2*6A to age-related hearing impairment

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of human TMHS cause recessively inherited non-syndromic hearing loss

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cochlear molecules and hereditary deafness

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/19030898

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00439-008-0596-3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

PubMed publication ID

19030898

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19030898

retrieved

14 March 2018

reference URL

http://europepmc.org/abstract/MED/19030898

ResearchGate publication ID

23494778

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