Genetic analysis of the ATP11B gene in Chinese Han population with cerebral small vessel disease

BACKGROUND: A loss-of-function mutation in ATPase phospholipid transporting 11-B (putative) (ATP11B) gene causing cerebral small vessel disease (SVD) in vivo, and a single intronic nucleotide polymorphism in ATP11B: rs148771930 that was associated with white matter hyperintensities burden in Europea...

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Detalles Bibliográficos
Autores principales: Yu, Wen-Kai, Wang, Yun-Chao, Gao, Yuan, Shi, Chang-He, Fan, Yu, Yu, Lu-Lu, Zhao, Zi-Chen, Li, Shan-Shan, Xu, Yu-Ming, Li, Yu-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746074/
https://www.ncbi.nlm.nih.gov/pubmed/36510145
http://dx.doi.org/10.1186/s12864-022-09051-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9746074/
https://www.ncbi.nlm.nih.gov/pubmed/36510145
http://dx.doi.org/10.1186/s12864-022-09051-0

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