Spinocerebellar ataxia type 6: founder effect in Western Japan (Q73667241)

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5 November 2019

title

Spinocerebellar ataxia type 6: founder effect in Western Japan (English)

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5 November 2019

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spinocerebellar ataxia type 6

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M Mori

1

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5 November 2019

Y Adachi

series ordinal

2

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5 November 2019

M Kusumi

series ordinal

3

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5 November 2019

K Nakashima

series ordinal

4

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5 November 2019

publication date

1 March 2001

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Journal of the Neurological Sciences

5 November 2019

number of pages

5

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based on heuristic

inferred from page(s)

published in

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5 November 2019

volume

185

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5 November 2019

issue

1

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5 November 2019

page(s)

43-47

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

5 November 2019

cites work

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Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

7 January 2021

1 reference

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CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

7 January 2021

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Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p

7 January 2021

1 reference

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Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900453-1

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900453-1

Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

7 January 2021

1 reference

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

7 January 2021

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Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families

7 January 2021

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Analysis of spinocerebellar ataxia types 1, 2, 3, and 6, dentatorubral-pallidoluysian atrophy, and Friedreich's ataxia genes in spinocerebellar ataxia patients in the UK.

7 January 2021

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Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

7 January 2021

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Clinical and molecular features of spinocerebellar ataxia type 6

7 January 2021

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Frequency of spinocerebellar ataxia types 1,2,3,6,7 and dentatorubral pallidoluysian atrophy mutations in Korean patients with spinocerebellar ataxia

7 January 2021

1 reference

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Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

7 January 2021

1 reference

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Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900453-1

Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion

7 January 2021

1 reference

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Frequency analysis of autosomal dominant cerebellar ataxias in Japanese patients and clinical characterization of spinocerebellar ataxia type 6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900453-1

A genetic epidemiological study of spinocerebellar ataxias in Tottori prefecture, Japan

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2801%2900453-1

Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families

7 January 2021

1 reference

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10.1016/S0022-510X(01)00453-1

7 January 2021

Identifiers

DOI

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5 November 2019

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