Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease-Reference-Cited by-同舟云学术

Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: Evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's disease

Published:2005-07 Issue:1-2 Volume:382 Page:191-194
ISSN:0304-3940
Container-title:Neuroscience Letters
language:en
Short-container-title:Neuroscience Letters

Author:

Simon-Sanchez Javier,Hanson Melissa,Singleton Amanda,Hernandez Dena,McInerney Aideen,Nussbaum Robert,Werner John,Gallardo Marisol,Weiser Roberto,Gwinn-Hardy Katrina,Singleton Andrew B.,Clarimon Jordi

Publisher

Elsevier BV

Subject

General Neuroscience

Reference10 articles.

1. SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings;Furtado;Neurology,2002

2. Genetics of Parkinson's disease;Gasser;J. Neurol.,2001

3. Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese;Gwinn-Hardy;Neurology,2000

4. Spinocerebellar ataxia type 3 phenotypically resembling parkinson disease in a black family;Gwinn-Hardy;Arch. Neurol.,2001

5. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases;Hughes;J. Neurol. Neurosurg. Psychiatry,1992

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