(Q34319769)

1 August 2017

title

Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. (English)

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spinocerebellar ataxia type 5

1 August 2017

main subject

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L P Ranum

1

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1 August 2017

L J Schut

2

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1 August 2017

J K Lundgren

3

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1 August 2017

H T Orr

4

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1 August 2017

D M Livingston

5

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1 August 2017

language of work or name

English

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publication date

1 November 1994

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1 August 2017

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1 August 2017

volume

8

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1 August 2017

issue

3

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1 August 2017

page(s)

280-284

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

1 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

Integrated human genome-wide maps constructed using the CEPH reference panel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

The 1993-94 Généthon human genetic linkage map

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

A family with hereditary ataxia: HLA typing

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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%2FNG1194-280

7 January 2021

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

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https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

The natural history of Machado-Joseph disease. An analysis of 138 personally examined cases.

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Machado-Joseph disease: an autosomal dominant motor system degeneration

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

HIV or zidovudine myopathy?

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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%2FNG1194-280

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%2FNG1194-280

7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

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%2FNG1194-280

7 January 2021

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Guidelines for human linkage maps: an international system for human linkage maps (ISLM, 1990).

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG1194-280

7 January 2021

Identifiers

DOI

10.1038/NG1194-280

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1 August 2017

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