An atypical ALS with PSP-like symptoms caused by ANXA11 p.D40G mutation: A case report and literature review

BACKGROUND: ANXA11 mutations were first reported to be associated with amyotrophic lateral sclerosis (ALS) in 2017. Several studies have investigated the prevalence of ANXA11 mutations in different populations, while less is known about the spectrum of phenotypes and the genotype–phenotype correlati...

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Detalles Bibliográficos
Autores principales: Zhang, Xin, Gao, Juan, Chi, Chunling, Zhao, Zhenzhen, Chan, Piu, Ma, Jinghong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978770/
https://www.ncbi.nlm.nih.gov/pubmed/36873447
http://dx.doi.org/10.3389/fneur.2023.1086264

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9978770/
https://www.ncbi.nlm.nih.gov/pubmed/36873447
http://dx.doi.org/10.3389/fneur.2023.1086264

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