A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7-Reference-Cited by-同舟云学术

A comprehensive clinical and genetic study of a large Mexican population with spinocerebellar ataxia type 7

Published:2014-10-16 Issue:1 Volume:16 Page:11-21
ISSN:1364-6745
Container-title:neurogenetics
language:en
Short-container-title:Neurogenetics

Author:

Velázquez-Pérez L.,Cerecedo-Zapata C. M.,Hernández-Hernández O.,Martínez-Cruz E.,Tapia-Guerrero Y. S.,González-Piña R.,Salas-Vargas J.,Rodríguez-Labrada R.,Gurrola-Betancourth R.,Leyva-García N.,Cisneros B.,Magaña J. J.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10048-014-0424-y.pdf

Reference49 articles.

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3. Garden GA, La Spada AR (2008) Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration. Cerebellum 7(2):138–149

4. David G, Abbas N, Stevanin G et al (1997) Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet 17(1):65–70

5. Martin J, Van Regemorter N, Del-Favero J et al (1999) Spinocerebellar ataxia type 7 (SCA7)—correlations between phenotype and genotype in one large Belgian family. J Neurol Sci 168(1):37–46

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