Andersen, P S <br/><br/>
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.  [electronic resource] 

 -  Journal of medical genetics  Dec 2001 
 - E43 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.38.12.e43  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Cardiomyopathy, Hypertrophic--epidemiology<br/>DNA Mutational Analysis<br/>Echocardiography<br/>Exons--genetics<br/>Female<br/>Gene Frequency--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Mutation, Missense--genetics<br/>Myosin Light Chains--genetics<br/>Netherlands--epidemiology<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>South Africa--epidemiology