A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family (Q47692150)

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scientific article published in August 1998

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English	A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family	scientific article published in August 1998

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instance of

scholarly article

1 reference

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Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

title

A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

main subject

long QT syndrome

1 reference

based on heuristic

inferred from title

author name string

Ackerman MJ

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Schroeder JJ

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Berry R

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Schaid DJ

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Porter CJ

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Michels VV

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Thibodeau SN

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

language of work or name

English

0 references

publication date

1 August 1998

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

published in

Pediatric Research

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

volume

44

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

page(s)

148-153

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

cites work

Ion channels--basic science and clinical disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

The long QT syndrome: ion channel diseases of the heart

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Identification of a family with inherited long QT syndrome after a pediatric near-drowning

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Use of cyclosporin A in establishing Epstein-Barr virus-transformed human lymphoblastoid cell lines

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

KCNE1 mutations cause Jervell and Lange-Nielsen syndrome

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Dominant-Negative KvLQT1 Mutations Underlie the LQT1 Form of Long QT Syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Lidocaine block of LQT-3 mutant human Na+ channels

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1203%2F00006450-199808000-00002

retrieved

21 January 2018

Identifiers

DOI

10.1203/00006450-199808000-00002

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

Dimensions Publication ID

1064213680

0 references

PubMed publication ID

9702906

1 reference

stated in

Europe PubMed Central

PubMed publication ID

9702906

retrieved

4 February 2018

reference URL

http://europepmc.org/abstract/MED/9702906

 

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