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1: J Med Genet. 2001 Dec;38(12):E43.Click here to read Click here to read Links

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.

PMID: 11748309 [PubMed - indexed for MEDLINE]

PMCID: PMC1734772