Boyden, Steven E <br/><br/>
Efficient identification of novel mutations in patients with limb girdle muscular dystrophy.  [electronic resource] 

 -  Neurogenetics  Oct 2010 
 - 449-55 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1364-6753 
<br/><br/><label>Standard No.: </label>10.1007/s10048-010-0250-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Age of Onset<br/>Child<br/>Child, Preschool<br/>Consanguinity<br/>Family Health<br/>Female<br/>Genetic Linkage<br/>Genotype<br/>Homozygote<br/>Humans<br/>Infant<br/>Lod Score<br/>Male<br/>Muscular Dystrophies, Limb-Girdle--genetics<br/>Mutation<br/>Pedigree<br/>Saudi Arabia