MYH7 p.(Arg1712Gln) is pathogenic founder variant causing hypertrophic cardiomyopathy with overall relatively delayed onset.
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Marsili L, et al. Among authors: russo f.
Neth Heart J. 2023 Aug;31(7-8):300-307. doi: 10.1007/s12471-023-01798-9. Epub 2023 Jul 24.
Neth Heart J. 2023.
PMID: 37488328
Free PMC article.