Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region (Q35889380)

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scientific article published in May 1994

Language	Label	Description	Also known as
English	Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region	scientific article published in May 1994

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scholarly article

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26 October 2019

Confirmation of the SCA-2 locus as an alternative locus for dominantly inherited spinocerebellar ataxias and refinement of the candidate region (English)

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26 October 2019

9

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Rouleau GA

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10 August 2017

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26 October 2019

author name string

Lopes-Cendes I

1

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26 October 2019

Andermann E

2

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26 October 2019

Attig E

3

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26 October 2019

Cendes F

4

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26 October 2019

Bosch S

5

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26 October 2019

Wagner M

6

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26 October 2019

Gerstenbrand F

7

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26 October 2019

Andermann F

8

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26 October 2019

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publication date

1 May 1994

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26 October 2019

American Journal of Human Genetics

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26 October 2019

54

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26 October 2019

5

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26 October 2019

774-781

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26 October 2019

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

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11 July 2018

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Strategies for multilocus linkage analysis in humans

1 reference

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11 July 2018

A new form of heredo-familial spinocerebellar degeneration with slow eye movements (nine families)

1 reference

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11 July 2018

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

1 reference

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Prevalence and occurrence of some rare neurological diseases in Iceland

1 reference

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11 July 2018

Spinocerebellar ataxia: localization of an autosomal dominant locus between two markers on human chromosome 6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Energy metabolism in disorders of the nervous system.

1 reference

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11 July 2018

Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba

1 reference

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11 July 2018

Dinucleotide repeat polymorphism at the D6S89 locus

1 reference

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11 July 2018

Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps telomeric to the HLA complex and is closely linked to the D6S89 locus in three large kindreds

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Cerebrospinal fluid as a reflector of central cholinergic and amino acid neurotransmitter activity in cerebellar ataxia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Tight linkage of the gene for spinocerebellar ataxia to D6S89 on the short arm of chromosome 6 in a kindred for which close linkage to both HLA and F13A1 is excluded

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Autosomal dominant spinocerebellar ataxia: locus heterogeneity in a Nebraska kindred

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Spinocerebellar ataxia (SCA1) in two large Italian kindreds: evidence in favour of a locus position distal to GLO1 and the HLA cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Thiamine status in inherited degenerative ataxias

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

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Linkage mapping of melanoma (MLM) using 172 microsatellite markers

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11 July 2018

A 17th-century founder gives rise to a large north American pedigree of autosomal dominant spinocerebellar ataxia not linked to the SCA1 locus on chromosome 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Genetic linkage and spinocerebellar ataxia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

HLA and complement typing in olivo-ponto-cerebellar atrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

HLA-Determination in Families with Hereditary Ataxia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1918266

11 July 2018

Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French families

1 reference

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24 September 2018

Glutamate dehydrogenase deficiency in patients with olivopontocerebellar atrophy

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

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Letter: Hereditary ataxia and HL-A genotypes

1 reference

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Brain choline acetyltransferase reduction in dominantly inherited olivopontocerebellar atrophy

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24 September 2018

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

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A family with hereditary ataxia: HLA typing

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage in hereditary ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A linkage study of hereditary ataxias and related disorders. Evidence of heterogeneity of dominant cerebellar ataxia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia in a large kindred: age at onset, reproduction, and genetic linkage studies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

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Anticipation in spinocerebellar ataxia type 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

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[Contribution to the problem of familial atrophy of the cerebellum.]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary cerebellar ataxia and genetic linkage with HLA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant cerebellar phenotypes: the genotype will settle the issue

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary ataxias: epidemiological aspects

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spinocerebellar ataxia: multipoint linkage analysis of genes associated with the disease locus

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Machado-Joseph disease locus is different from the spinocerebellar ataxia locus (SCA1)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8178818

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8178818%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8178818%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

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