Richard, I <br/><br/>
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.  [electronic resource] 

 -  American journal of human genetics  May 1997 
 - 1128-38 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Calpain--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 15<br/>Europe<br/>Female<br/>Genetic Heterogeneity<br/>Genetic Markers<br/>Haplotypes<br/>Humans<br/>Isoenzymes--genetics<br/>Lod Score<br/>Male<br/>Middle East<br/>Muscle Proteins<br/>Muscular Dystrophies--classification<br/>Mutation<br/>Pedigree<br/>United States