Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia-Reference-Cited by-同舟云学术

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Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Published:2019-06-26 Issue:1 Volume:8 Page:
ISSN:2047-9158
Container-title:Translational Neurodegeneration
language:en
Short-container-title:Transl Neurodegener

Author:

Wei Qiao,Dong Hai-Lin,Pan Li-Ying,Chen Cong-Xin,Yan Yang-Tian,Wang Rou-Min,Li Hong-Fu,Liu Zhi-Jun,Tao Qing-Qing,Wu Zhi-Ying

Funder

National Natural Science Foundation of China

Research foundation for distinguished scholar of Zhejiang University

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience,Clinical Neurology

Link

http://link.springer.com/content/pdf/10.1186/s40035-019-0157-9.pdf

Reference49 articles.

1. Fink JK. Hereditary spastic paraplegia. Curr Neurol Neurosci Rep. 2006;6(1):65–76.

2. Fink JK. Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms. Acta Neuropathol. 2013;126(3):307–28.

3. Harding AE. Classification of the hereditary ataxias and paraplegias. Lancet. 1983;1(8334):1151–5.

4. Tesson C, Koht J, Stevanin G. Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology. Hum Genet. 2015;134(6):511–38.

5. Erichsen AK, Koht J, Stray-Pedersen A, Abdelnoor M, Tallaksen CM. Prevalence of hereditary ataxia and spastic paraplegia in Southeast Norway: a population-based study. Brain. 2009;132(Pt 6):1577–88.

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