The Involvement of ALPK3 in Hypertrophic Cardiomyopathy in East Asia

OBJECTIVE: ALPK3 is associated with a recessive form of pediatric cardiomyopathy accompanied by musculoskeletal and craniofacial abnormalities. Heterozygous truncating variants in this gene (ALPK3tv) have recently been confirmed as a cause of autosomal dominant hypertrophic cardiomyopathy (HCM). Whe...

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Detalles Bibliográficos
Autores principales: Dai, Jiaqi, Li, Ke, Huang, Man, Sun, Yang, Liu, Hao, Li, Zongzhe, Chen, Peng, Wang, Hong, Wu, Dongyang, Chen, Yanghui, Xiao, Lei, Wei, Haoran, Li, Rui, Peng, Liyuan, Yu, Ting, Wang, Yan, Wang, Dao Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240616/
https://www.ncbi.nlm.nih.gov/pubmed/35783621
http://dx.doi.org/10.3389/fmed.2022.915649

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9240616/
https://www.ncbi.nlm.nih.gov/pubmed/35783621
http://dx.doi.org/10.3389/fmed.2022.915649

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