Molecular analysis of spinocerebellar ataxia trinucleotide repeat behavior in normal individuals of a Brazilian population-Reference-Cited by-同舟云学术

Molecular analysis of spinocerebellar ataxia trinucleotide repeat behavior in normal individuals of a Brazilian population

Published:2008-06 Issue:1-2 Volume:269 Page:113-117
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

de Vargas Wolfgramm Eldamária,de Carvalho Fernanda Magri,De Nadai Sartori Mariana Penha,Spagnol Perrone Ângela Maria,de Paula Flávia,Louro Iúri Drumond

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

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3. Other causes of ataxia in patients with SCA mutations;Dawson;Clin Neurol Neurosurg,2007

4. Diagnosis of five spinocerebellar ataxia disorders by multiplex amplification and capillary electrophoresis;Dorschner;J Mol Diagn,2002

5. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schöls;Lancet Neurol,2004

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