Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2-Reference-Cited by-同舟云学术

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Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2

Published:2007-12 Issue:1-2 Volume:263 Page:158-164
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Velázquez Pérez Luis,Sánchez Cruz Gilberto,Canales Ochoa Nalia,Rodríguez Labrada Roberto,Rodríguez Díaz Julio,Almaguer Mederos Luis,Laffita Mesa José

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference36 articles.

1. Clinical features and classification of inherited ataxias;Harding,1993

2. Expansion of an unstable trinucleotide CAG repeats in spinocerebellar ataxia type 1;Orr;Nat Genet,1993

3. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats;Imbert;Nat Genet,1996

4. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2;Pulst;Nat Genet,1996

5. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT;Sanpei;Nat Genet,1996

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