(Q41516217)

2 October 2017

title

Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. (English)

1 reference

2 October 2017

main subject

spinocerebellar ataxia

1 reference

5

Zoghbi HY

1 reference

2 October 2017

Chung MY

1

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2 October 2017

Ranum LP

2

1 reference

2 October 2017

Duvick LA

3

1 reference

2 October 2017

Servadio A

4

1 reference

2 October 2017

Orr HT

6

1 reference

2 October 2017

language of work or name

English

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publication date

1 November 1993

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2 October 2017

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2 October 2017

volume

5

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2 October 2017

issue

3

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2 October 2017

page(s)

254-258

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

2 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Dynamic mutations: a new class of mutations causing human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

Spinocerebellar ataxia: study of a large kindred. I. General information and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

A family with hereditary ataxia: HLA typing

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Spinocerebellar ataxia: variable age of onset and linkage to human leukocyte antigen in a large kindred.

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Linkage studies in spinocerebellar ataxia (SCA)

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Linkage studies on glyoxalase I (GLO), pepsinogen (PG), spinocerebellar ataxia (SCA1), and HLA

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Trinucleotide repeat polymorphism in the androgen receptor gene (AR).

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG1193-254

7 January 2021

Identifiers

DOI

10.1038/NG1193-254

1 reference

Dimensions Publication ID

2 October 2017

1047008556

0 references

1 reference