Molecular and clinical characteristics of ATP1A3-related diseases

OBJECTIVE: With detailed studies of ATP1A3-related diseases, the phenotypic spectrum of ATP1A3 has greatly expanded. This study aimed to potentially identify the mechanisms by which ATP1A3 caused neurological dysfunction by analyzing the clinical features and phenotypes of ATP1A3-related diseases, a...

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Detalles Bibliográficos
Autores principales: Li, Yinchao, Liu, Xianyue, Wang, Chengzhe, Su, Zhengwei, Zhao, Ke, Yang, Man, Chen, Shuda, Zhou, Liemin
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/PMC9373902/
https://www.ncbi.nlm.nih.gov/pubmed/35968298
http://dx.doi.org/10.3389/fneur.2022.924788

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9373902/
https://www.ncbi.nlm.nih.gov/pubmed/35968298
http://dx.doi.org/10.3389/fneur.2022.924788

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