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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...
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| Published in: | BMC Cardiovasc Disord |
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| Main Authors: | , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
BioMed Central
2018
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| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6029398/ https://ncbi.nlm.nih.gov/pubmed/29969989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12872-018-0867-4 |
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