Spinocerebellar ataxia type 5 in a family descended from the grandparents of President Lincoln maps to chromosome 11. (Q34319769)

1 August 2017

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

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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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8

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3

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1 August 2017

280-284

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https://scigraph.springernature.com/pub.10.1038/ng1194-280

1 August 2017

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

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

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

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

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Machado-Joseph disease: an autosomal dominant motor system degeneration

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Spinocerebellar ataxia and HLA linkage: risk prediction by HLA typing

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HIV or zidovudine myopathy?

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

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

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

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

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

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

Identifiers

DOI

10.1038/NG1194-280

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1 August 2017

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