Mutations in the profilin 1 gene are not common in amyotrophic lateral sclerosis of Chinese origin-Reference-Cited by-同舟云学术

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Mutations in the profilin 1 gene are not common in amyotrophic lateral sclerosis of Chinese origin

Published:2013-06 Issue:6 Volume:34 Page:1713.e5-1713.e6
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Zou Zhang-Yu,Sun Qing,Liu Ming-Sheng,Li Xiao-Guang,Cui Li-Ying

Funder

National Natural Science Foundation of China

International Cooperation and Exchange National Natural Science Foundation of China

Innovation Fund of the Chinese Academy of Medical Sciences and Peking Union Medical College

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Clinical Neurology,Ageing,General Neuroscience

Cited by 28 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. FUS mutation is probably the most common pathogenic gene for JALS, especially sporadic JALS;Revue Neurologique;2021-04

2. The Occurrence of FUS Mutations in Pediatric Amyotrophic Lateral Sclerosis: A Case Report and Review of the Literature;Journal of Child Neurology;2020-04-13

3. Familial flail leg ALS caused by PFN1 mutation;Journal of Neurology, Neurosurgery & Psychiatry;2019-08-10

4. Therapeutic Dissolution of Aberrant Phases by Nuclear-Import Receptors;Trends in Cell Biology;2019-04

5. Clinical and Genetic Features of Patients with Juvenile Amyotrophic Lateral Sclerosis with Fused in Sarcoma (FUS) Mutation;Medical Science Monitor;2018-12-03

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