Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of MYOM2

BACKGROUND: Rare genetic variants have been identified to be important contributors to the risk of Tetralogy of Fallot (TOF), the most common cyanotic congenital heart disease (CHD). But relatively limited familial studies with small numbers of TOF cases have been reported to date. In this study, we...

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Detalles Bibliográficos
Autores principales: Wang, Jing, Wang, Chunyan, Xie, Haiyang, Feng, Xiaoyuan, Wei, Lei, Wang, Binbin, Li, Tengyan, Pi, Mingan, Gong, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300848/
https://www.ncbi.nlm.nih.gov/pubmed/35872890
http://dx.doi.org/10.3389/fcvm.2022.863650

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300848/
https://www.ncbi.nlm.nih.gov/pubmed/35872890
http://dx.doi.org/10.3389/fcvm.2022.863650

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