Whole-exome sequencing identifies R1279X of MYH6 gene to be associated with congenital heart disease

BACKGROUND: Myosin VI, encoded by MYH6, is expressed dominantly in human cardiac atria and plays consequential roles in cardiac muscle contraction and comprising the cardiac muscle thick filament. It has been reported that the mutations in the MYH6 gene associated with sinus venosus atrial septal de...

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Detalles Bibliográficos
Autores principales: Razmara, Ehsan, Garshasbi, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029398/
https://www.ncbi.nlm.nih.gov/pubmed/29969989
http://dx.doi.org/10.1186/s12872-018-0867-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029398/
https://www.ncbi.nlm.nih.gov/pubmed/29969989
http://dx.doi.org/10.1186/s12872-018-0867-4

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