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Logo of jmedgeneJournal of Medical GeneticsCurrent TOCInstructions for authors
 
J Med Genet. Dec 2001; 38(12): e43.
PMCID: PMC1734772
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations
P. S. Andersen, O. Havndrup, H. Bundgaard, J. C. Moolman-Smook, L. A. Larsen, J. Mogensen, P. A. Brink, A. D. Borglum, V. A. Corfield, K. Kjeldsen, J. Vuust, and M. Christiansen
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