Weiler, T <br/><br/>
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).  [electronic resource] 

 -  Human molecular genetics  May 1999 
 - 871-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/8.5.871  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Biopsy<br/>Canada<br/>Dysferlin<br/>Female<br/>Haplotypes<br/>Homozygote<br/>Humans<br/>Indians, North American--genetics<br/>Male<br/>Membrane Proteins<br/>Molecular Sequence Data<br/>Muscle Proteins--genetics<br/>Muscle, Skeletal--metabolism<br/>Muscular Dystrophies--genetics<br/>Mutation<br/>Mutation, Missense<br/>Pedigree