SCA2 is not a major locus for ADCA type I in French families
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference14 articles.
1. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus
2. Phenotypic variability in autosomal dominant cerebellar ataxia type I is unrelated to genetic heterogeneity
3. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1
4. (1993): Clinical features and classification of inherited ataxias. In (eds): “Inherited Ataxias—Advances in Neurology 61.” New York: Raven Press, pp 1-14.
5. Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1
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1. FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion;Acta Neuropathologica;2014-04-10
2. Spinocerebellar Ataxia Type 2 Presenting With Cognitive Regression in Childhood;Journal of Child Neurology;2008-02-20
3. Polyneuropathy in autosomal dominant cerebellar ataxias: Phenotype-genotype correlation;Muscle & Nerve;1999-06
4. A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis;Brain;1998-12-01
5. Clinical Aspects of CAG Repeat Diseases;Brain Pathology;1997-07
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