‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization-Reference-Cited by-同舟云学术

‘Costa da Morte’ ataxia is spinocerebellar ataxia 36: clinical and genetic characterization

Published:2012-04-03 Issue:5 Volume:135 Page:1423-1435
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

García-Murias María,Quintáns Beatriz,Arias Manuel,Seixas Ana I.,Cacheiro Pilar,Tarrío Rosa,Pardo Julio,Millán María J.,Arias-Rivas Susana,Blanco-Arias Patricia,Dapena Dolores,Moreira Ramón,Rodríguez-Trelles Francisco,Sequeiros Jorge,Carracedo Ángel,Silveira Isabel,Sobrido María J.

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

Link

http://academic.oup.com/brain/article-pdf/135/5/1423/17348569/aws069.pdf

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3. Parent-of-origin differences of mutant HTT CAG repeat instability in Huntington’s disease;Aziz;Eur J Med Genet,2011

4. Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23;Bakalkin;Am J Hum Genet,2010

5. RNA gainof-function in spinocerebellar ataxia type 8;Daughters;PLoS Genet,2009

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