Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion-Reference-Cited by-同舟云学术

Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion

Published:2014-12-04 Issue:9 Volume:86 Page:986-995
ISSN:0022-3050
Container-title:Journal of Neurology, Neurosurgery & Psychiatry
language:en
Short-container-title:J Neurol Neurosurg Psychiatry

Author:

Obayashi Masato,Stevanin Giovanni,Synofzik Matthis,Monin Marie-Lorraine,Duyckaerts Charles,Sato Nozomu,Streichenberger Nathalie,Vighetto Alain,Desestret Virginie,Tesson Christelle,Wichmann H-Erich,Illig Thomas,Huttenlocher Johanna,Kita Yasushi,Izumi Yuishin,Mizusawa Hidehiro,Schöls Ludger,Klopstock Thomas,Brice Alexis,Ishikawa Kinya,Dürr Alexandra

Publisher

BMJ

Subject

Psychiatry and Mental health,Neurology (clinical),Surgery

Reference31 articles.

1. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Dürr;Lancet Neurol,2012

2. Mutations in KCND3 cause spinocerebellar ataxia type 22;Lee;Ann Neurol,2012

3. New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32;Serrano-Munuera;JAMA Neurol,2013

4. Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement;Kobayashi;Am J Hum Genet,2011

5. ‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization;García-Murias;Brain,2012

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