WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation

BACKGROUND: Congenital heart disease (CHD) is the most common birth defect and has high heritability. Although some susceptibility genes have been identified, the genetic basis underlying the majority of CHD cases is still undefined. METHODS: A total of 1320 unrelated CHD patients were enrolled in o...

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Detalles Bibliográficos
Autores principales: Hao, Lili, Ma, Jing, Wu, Feizhen, Ma, Xiaojing, Qian, Maoxiang, Sheng, Wei, Yan, Tizhen, Tang, Ning, Jiang, Xin, Zhang, Bowen, Xiao, Deyong, Qian, Yanyan, Zhang, Jin, Jiang, Nan, Zhou, Wenhao, Chen, Weicheng, Ma, Duan, Huang, Guoying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270576/
https://www.ncbi.nlm.nih.gov/pubmed/35808830
http://dx.doi.org/10.1002/ctm2.941

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9270576/
https://www.ncbi.nlm.nih.gov/pubmed/35808830
http://dx.doi.org/10.1002/ctm2.941

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