Spinocerebellar ataxia: relationship between phenotype and genotype - a review-Reference-Cited by-同舟云学术

Spinocerebellar ataxia: relationship between phenotype and genotype - a review

Published:2016-06-30 Issue:4 Volume:90 Page:305-314
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Sun Y.-M.¹,Lu C.²³,Wu Z.-Y.²⁴

Affiliation:

1. Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College; Fudan University; Shanghai China

2. Department of Neurology and Research Center of Neurology in Second Affiliated Hospital, the Collaborative Innovation Center for Brain Science; Zhejiang University School of Medicine; Hangzhou China

3. Department of Neurology and Institute of Neurology, First Affiliated Hospital; Fujian Medical University; Fuzhou China

4. Joint Institute for Genetics and Genome Medicine between Zhejiang University and University of Toronto; Zhejiang University; Hangzhou China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference124 articles.

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

4. The global epidemiology of hereditary ataxia and spastic paraplegia: a systematic review of prevalence studies;Ruano;Neuroepidemiology,2014

5. Clinical features, neurogenetics and neuropathology of the polyglutamine spinocerebellar ataxias type 1, 2, 3, 6 and 7;Rub;Prog Neurobiol,2013

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