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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...
Autores principales: | Razmara, Ehsan, Garshasbi, Masoud |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
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 |
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