Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population-Reference-Cited by-同舟云学术

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Friedreich's Ataxia (FRDA) is an extremely rare cause of autosomal recessive ataxia in Chinese Han population

Published:2015-04 Issue:1-2 Volume:351 Page:124-126
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Zeng Junsheng^ORCID,Wang Junling,Zeng Sheng,He Miao,Zeng Xianfeng,Zhou Yao,Liu Zhen,Jiang Hong,Tang Beisha

Funder

National Natural Science Foundation of China

National Department Public Benefit Research Foundation

National Science & Technology Pillar Program

Fundamental Research Funds for the Central Universities

Research Fund for the Doctoral Program of Higher Education of China

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

Reference15 articles.

1. Clinical neurogenetics: Friedreich ataxia;Collins;Neurol Clin,2013

2. Typical Friedreich's ataxia without GAA expansions and GAA expansion without typical Friedreich's ataxia;McCabe;J Neurol,2000

3. Friedreich's ataxia;Pearce;J Neurol Neurosurg Psychiatry,2004

4. Clinical features of Friedreich's ataxia: classical and atypical phenotypes;Parkinson;J Neurochem,2013

5. Friedreich ataxia in Acadian families from eastern Canada: clinical diversity with conserved haplotypes;Richter;Am J Med Genet,1996

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