(Q74481409)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

SCA6 mutation analysis in a large cohort of the Japanese patients with late-onset pure cerebellar ataxia (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

I Yabe

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

H Sasaki

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

T Matsuura

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

A Takada

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

A Wakisaka

5

1 reference

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11 November 2019

Y Suzuki

6

1 reference

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11 November 2019

T Fukazawa

7

1 reference

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11 November 2019

T Hamada

8

1 reference

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11 November 2019

T Oda

9

1 reference

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11 November 2019

A Ohnishi

10

1 reference

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11 November 2019

K Tashiro

11

1 reference

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11 November 2019

publication date

1 January 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

Journal of the Neurological Sciences

11 November 2019

published in

1 reference

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11 November 2019

volume

156

1 reference

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11 November 2019

issue

1

1 reference

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11 November 2019

page(s)

89-95

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

The gene for autosomal dominant cerebellar ataxia with pigmentary macular dystrophy maps to chromosome 3p12–p21.1

11 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Dentatorubral-pallidoluysian atrophy and Haw River syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Autosomal dominant pure cerebellar ataxia. Neurological and genetic study

7 January 2021

1 reference

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Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p.

7 January 2021

1 reference

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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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Autosomal dominant pure cerebellar ataxia. A clinical and genetic analysis of eight Japanese families.

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

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Distribution and functional significance of the P-type, voltage-dependent Ca2+ channels in the mammalian central nervous system

7 January 2021

1 reference

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Evidence for the existence of a fourth dominantly inherited spinocerebellar ataxia locus

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Primary structure and functional expression from complementary DNA of a brain calcium channel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Dominantly inherited cerebello-olivary atrophy is not due to a mutation at the spinocerebellar ataxia-I, Machado-Joseph disease, or Dentato-Rubro-Pallido-Luysian atrophy locus.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Spinocerebellar ataxia 1 (SCA1) in the Japanese: analysis of CAG trinucleitide repeat expansion and instability of the repeat for paternal transmission

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

Evidence for inter-generational instability in the CAG repeat in the MJD1 gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

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%2898%2900009-4

Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900009-4

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0022-510X(98)00009-4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9559993%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference