Phenotype of VCP Mutations in Chinese Amyotrophic Lateral Sclerosis Patients

Mutations in the valosin-containing protein (VCP) gene have been linked to amyotrophic lateral sclerosis (ALS) in the Caucasian populations. However, the phenotype of VCP mutations in Chinese patients with (ALS) remains unclear. Targeted next-generation sequencing covered 28 ALS-related genes includ...

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Detalles Bibliográficos
Autores principales: Feng, Shu-Yan, Lin, Han, Che, Chun-Hui, Huang, Hua-Pin, Liu, Chang-Yun, Zou, Zhang-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858817/
https://www.ncbi.nlm.nih.gov/pubmed/35197922
http://dx.doi.org/10.3389/fneur.2022.790082

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8858817/
https://www.ncbi.nlm.nih.gov/pubmed/35197922
http://dx.doi.org/10.3389/fneur.2022.790082

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