Identification of an A4V SOD1 mutation in a Chinese patient with amyotrophic lateral sclerosis without the A4V founder effect common in North America-Reference-Cited by-同舟云学术

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Identification of an A4V SOD1 mutation in a Chinese patient with amyotrophic lateral sclerosis without the A4V founder effect common in North America

Published:2018-03-22 Issue:5-6 Volume:19 Page:466-468
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Tang Lu¹,Ma Yan¹,Liu Xiaolu¹,Chen Lu¹,Fan Dongsheng¹

Affiliation:

1. Department of Neurology, Peking University Third Hospital, Beijing, PR China

Funder

National Natural Science Foundation of China

Peking University-Ulm University Union Foundation

Natural Science Foundation of Beijing Municipality

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2018.1451895

Reference10 articles.

1. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

2. ALSoD: A user-friendly online bioinformatics tool for amyotrophic lateral sclerosis genetics

3. C9orf72 repeat expansions are not detected in Chinese patients with familial ALS

4. C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis

5. Analysis of SOD1 mutations in a Chinese population with amyotrophic lateral sclerosis: a case-control study and literature review

Cited by 3 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. A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations;Translational Neurodegeneration;2021-10-28

2. Haplotype Analysis of the First A4V-SOD1 Spanish Family: Two Separate Founders or a Single Common Founder?;Frontiers in Genetics;2019-11-08

3. Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis;Aging and disease;2019

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