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First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia a...

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia a...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1900350155

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China

About this item

Full title

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China

Publisher

United States: Public Library of Science

Journal title

PloS one, 2017-05, Vol.12 (5), p.e0177955-e0177955

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Spinocerebellar ataxia type 10 (SCA10) is an autosomal-dominant cerebellar ataxia that is variably accompanied by epilepsy and other neurological disorders. It is caused by an expansion of the ATTCT pentanucleotide repeat in intron 9 of the ATXN10 gene. Until now, SCA10 was almost exclusively found in the American continents, while no cases had bee...

Alternative Titles

Full title

First report of a Japanese family with spinocerebellar ataxia type 10: The second report from Asia after a report from China

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1900350155

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1900350155

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0177955

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