Genotype-phenotype association and functional analysis of <i>hnRNPA1</i> mutations in amyotrophic lateral sclerosis-Reference-Cited by-同舟云学术

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Genotype-phenotype association and functional analysis of hnRNPA1 mutations in amyotrophic lateral sclerosis

Published:2024-05-08 Issue:5-6 Volume:25 Page:600-607
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Zhang Xinyi¹²,Sun Ye¹,Zhang Xinzhe²,Shen Dongchao¹,Shu Shi¹,Yang Xunzhe¹,Liu Mingsheng¹,Cui Liying¹,Liu Qing¹,Zhang Xue²

Affiliation:

1. Department of Neurology, Peking Union Medical College Hospital, Peking Union Medical College (PUMC) & Chinese Academy of Medical Science (CAMS), Beijing, China and

2. Mckusick-Zhang Center for Genetic Medicine, State Key Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, PUMC & CAMS, Beijing, China

Funder

National High Level Hospital Clinical Research Funding

National Key Research and Development Program of China

National Natural Science Foundation of China

CAMS Innovation Fund for Medical Sciences

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2024.2346502

Reference35 articles.

1. Amyotrophic Lateral Sclerosis

2. ALS Genetics, Mechanisms, and Therapeutics: Where Are We Now?

3. ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia

4. The epidemiology and genetics of Amyotrophic lateral sclerosis in China

5. Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis

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