Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients-Reference-Cited by-同舟云学术

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Published:2009-08-20 Issue:10 Volume:132 Page:2688-2698
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Anheim M.,Monga B.,Fleury M.,Charles P.,Barbot C.,Salih M.,Delaunoy J. P.,Fritsch M.,Arning L.,Synofzik M.,Schöls L.,Sequeiros J.,Goizet C.,Marelli C.,Le Ber I.,Koht J.,Gazulla J.,De Bleecker J.,Mukhtar M.,Drouot N.,Ali-Pacha L.,Benhassine T.,Chbicheb M.,M’Zahem A.,Hamri A.,Chabrol B.,Pouget J.,Murphy R.,Watanabe M.,Coutinho P.,Tazir M.,Durr A.,Brice A.,Tranchant C.,Koenig M.

Publisher

Oxford University Press (OUP)

Subject

Neurology (clinical)

Link

http://academic.oup.com/brain/article-pdf/132/10/2688/13794678/awp211.pdf

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4. Identification and characterisation of a large Senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2);Arning;Neurogenetics,2008

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