(Q48844480)

16 February 2018

title

Central phenotype and related varieties of spinocerebellar ataxia 2 (SCA2): a clinical and genetic study with a pedigree in the Japanese. (English)

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16 February 2018

main subject

spinocerebellar ataxia

1 reference

Sasaki H

1

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16 February 2018

Fukazawa T

2

1 reference

16 February 2018

Wakisaka A

3

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16 February 2018

Hamada K

4

1 reference

16 February 2018

Hamada T

5

1 reference

16 February 2018

Koyama T

6

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16 February 2018

Tsuji S

7

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16 February 2018

Tashiro K

8

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16 February 2018

publication date

1 December 1996

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16 February 2018

Journal of the Neurological Sciences

number of pages

6

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based on heuristic

inferred from page(s)

published in

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16 February 2018

volume

144

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16 February 2018

issue

1-2

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16 February 2018

page(s)

176-181

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16 February 2018

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus

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Has spinocerebellar ataxia type 2 a distinct phenotype? Genetic and clinical study of an Italian family.

7 January 2021

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The 1993-94 Généthon human genetic linkage map

7 January 2021

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

7 January 2021

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Genetic heterogeneity of dominantly inherited olivopontocerebellar atrophy (OPCA) in the Japanese: linkage study of two pedigrees and evidence for the disease locus on chromosome 12q (SCA2)

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900225-0

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings.

7 January 2021

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

7 January 2021

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

7 January 2021

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Anticipation in spinocerebellar ataxia type 2

7 January 2021

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CAG repeat expansion of Machado-Joseph disease in the Japanese: analysis of the repeat instability for parental transmission, and correlation with disease phenotype.

7 January 2021

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Clinical features and natural history of spinocerebellar ataxia type 1

7 January 2021

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Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

7 January 2021

1 reference

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

7 January 2021

1 reference

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10.1016/S0022-510X(96)00225-0

7 January 2021

Identifiers

DOI

1 reference

16 February 2018

PubMed ID

8994121

1 reference

16 February 2018