SCA38 is rare in mainland China-Reference-Cited by-同舟云学术

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SCA38 is rare in mainland China

Published:2015-11 Issue:1-2 Volume:358 Page:333-334
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Liu Zhen,Zeng Sheng,Zeng Junsheng,Zhou Yao,Zeng Xianfeng,jiang Hong,Shen Lu,Tang Beisha,Wang Junling

Funder

Program of National Natural Science Foundation of China

National Department Public Benefit Research Foundation

Key Projects in the National Science & Technology Pillar Program during the Twelfth Five-year Plan Period

Fundamental Research Funds for the Central Universities

Doctoral Program of Higher Education of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference11 articles.

1. Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis;van de Warrenburg;Neurology,2002

2. Molecular epidemiology of spinocerebellar ataxia type 6;Craig;Ann. Neurol.,2004

3. ELOVL5 mutations cause spinocerebellar ataxia 38;Di Gregorio;Am. J. Hum. Genet.,2014

4. Clinical features and classification of inherited ataxias;Harding;Adv. Neurol.,1993

5. Regulation of hepatic fatty acid elongase 5 by LXRalpha-SREBP-1c;Qin;Biochim. Biophys. Acta,2009

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification of IFRD1 variant in a Han Chinese family with autosomal dominant hereditary spastic paraplegia associated with peripheral neuropathy and ataxia;Journal of Human Genetics;2018-01-23

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