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SOD1 Mutation Spectrum and Natural History of ALS Patients in a 15-Year Cohort in Southeastern China
Background: Mutations in superoxide dismutase 1 gene (SOD1) are the most frequent high penetrant genetic cause for amyotrophic lateral sclerosis (ALS) in the Chinese population. A detailed natural history of SOD1-mutated ALS patients will provide key information for ongoing genetic clinical trials....
Autores principales: | Chen, Lu-Xi, Xu, Hai-Feng, Wang, Pei-Shan, Yang, Xin-Xia, Wu, Zhi-Ying, Li, Hong-Fu |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551486/ https://www.ncbi.nlm.nih.gov/pubmed/34721532 http://dx.doi.org/10.3389/fgene.2021.746060 |
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