Exon 8–17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review-Reference-Cited by-同舟云学术

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Exon 8–17 deletions of SPAST in a Chinese family with hereditary spastic paraplegia: A case report and literature review

Published:2015-10 Issue:1-2 Volume:357 Page:282-284
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Wang Kang,Zhao Guohua

Funder

National Scientific Foundations of China

Chinese College Funds for Doctorate Degree

Excellent Young Doctor Funds of Zhejiang Health

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference20 articles.

1. Classification of the hereditary ataxias and paraplegia;Harding;Lancet,1983

2. Mutation in CPT1C associated with pure autosomal dominant spastic paraplegia;Rinaldi;JAMA Neurol.,2015

3. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia;Hazan;Nat. Genet.,1999

4. Mutation analysis of the spastin gene (SPG4) in patients in Germany with autosomal dominant hereditary spastic paraplegia;Sauter;Hum. Mutat.,2002

5. High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia;Beetz;Neurology,2006

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