ArticleExperimental and clinical cardiology2001

Familial hypertrophic cardiomyopathy owing to double heterozygosity for a 403Arg--> Trp mutation in exon 13 of the MYH7 gene and a novel mutation, 453Arg--> His, in exon 14 of the MYH7 gene: A case report.

R Haluza et al.PubMed ↗Full text ↗

No numbers read from the abstract.