Mutations in the tail domain of MYH3 contributes to atrial septal defect

Atrial septal defect (ASD) is one of the most common congenital heart defects diagnosed in children. Sarcomeric genes has been attributed to ASD and knockdown of MYH3 functionally homologues gene in chick models indicated abnormal atrial septal development. Here, we report for the first time, a case...

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Detalles Bibliográficos
Autores principales: Maran, Sathiya, Ee, Robson, Faten, Siti Aisyah, Sy Bing, Choi, Khaw, Kooi Yeong, Erin Lim, Swee-Hua, Lai, Kok-Song, Wan Ibrahim, Wan Pauzi, Mohd Zain, Mohd Rizal, Chan, Kok Gan, Gan, Siew Hua, Tan, Huay Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173802/
https://www.ncbi.nlm.nih.gov/pubmed/32315303
http://dx.doi.org/10.1371/journal.pone.0230982

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7173802/
https://www.ncbi.nlm.nih.gov/pubmed/32315303
http://dx.doi.org/10.1371/journal.pone.0230982

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