Articles with "myh7 splicing" as a keyword



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Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family

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Published in 2022 at "BMC Medical Genomics"

DOI: 10.1186/s12920-022-01186-z

Abstract: Background Left ventricular non-compaction cardiomyopathy (LVNC) is a rare congenital heart defect. Gene defections have been found in patients with LVNC and their family members; and MYH7 is the most frequent gene associated with LVNC.… read more here.

Keywords: variant allele; myh7 splicing; cardiac phenotypes; family ... See more keywords