Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis-Reference-Cited by-同舟云学术

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Clinical features and genotype-phenotype correlation analysis in patients with ATL1 mutations: A literature reanalysis

Published:2017-04-04 Issue:1 Volume:6 Page:
ISSN:2047-9158
Container-title:Translational Neurodegeneration
language:en
Short-container-title:Transl Neurodegener

Author:

Zhao Guo-hua,Liu Xiao-min

Funder

National Scientific Foundations of China

Natural Scientific Fundation of Zhejiang Province

Research Fundation of Zhejiang Health

Natural Science Foundation of Shandong Province

Key Research and Development Project of Shandong Province

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience,Neurology (clinical)

Link

http://link.springer.com/content/pdf/10.1186/s40035-017-0079-3.pdf

Reference60 articles.

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

2. Mc Dermott CJ, et al. Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry. 2000;69(2):150–60.

3. Gan-Or Z, et al. Mutations in CAPN1 cause autosomal- recessive hereditary spastic paraplegia. Am J Hum Genet. 2016;98(5):1038–46.

4. Hazan J, et al. Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia. Nat Genet. 1999;23(3):296–303.

5. Tallaksen CM, Durr A, Brice A. Recent advances in hereditary spastic paraplegia. Current Opinion Neurol. 2001;14:457–63.

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