Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
In conclusion, we identified several novel HCM‑causing MYH7 mutations. More importantly, this is the first study to report a rare HCM family with monoallelic double mutations.
PMID: 31638223 [PubMed - as supplied by publisher]
Source: Molecular Medicine Reports - Category: Molecular Biology Tags: Mol Med Rep Source Type: research
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