QuickView for MHC;jsessionid=19234C71588E6F4EBB437238171ECF3F;jsessionid=6FBFF899D260B0DE050D13C893787C4F (gene)

1. Recent research on childhood hypertrophic cardiomyopathy caused by MYH7 gene mutations].
2. Long-Term Prevalence of Systolic Dysfunction in MYBPC3 Versus MYH7-Related Hypertrophic Cardiomyopat…
3. Left ventricular non-compaction cardiomyopathy: restrictive subtype with MYH7 gene mutation.
4. MYH7 variants cause complex congenital heart disease.
5. Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy us…

There were no clinical trials for MHC;jsessionid=19234C71588E6F4EBB437238171ECF3F;jsessionid=6FBFF899D260B0DE050D13C893787C4F