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

J Med Genet. 2001 Dec;38(12):E43. doi: 10.1136/jmg.38.12.e43.

Authors

P S Andersen, O Havndrup, H Bundgaard, J C Moolman-Smook, L A Larsen, J Mogensen, P A Brink, A D Børglum, V A Corfield, K Kjeldsen, J Vuust, M Christiansen

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
Adult
Aged
Cardiomyopathy, Hypertrophic / epidemiology
Cardiomyopathy, Hypertrophic / genetics*
Cardiomyopathy, Hypertrophic / physiopathology*
DNA Mutational Analysis
Echocardiography
Exons / genetics
Female
Gene Frequency / genetics*
Humans
Male
Middle Aged
Mutation / genetics*
Mutation, Missense / genetics
Myosin Light Chains / genetics*
Netherlands / epidemiology
Pedigree
Phenotype
Polymorphism, Single-Stranded Conformational
South Africa / epidemiology

Substances

Myosin Light Chains