Busquets, C <br/><br/>
Evidence of a single origin for the most frequent mutation (R402W) causing glutaryl-CoA dehydrogenase deficiency: identification of 3 novel polymorphisms and haplotype definition.  [electronic resource] 

 -  Human mutation  Feb 2000 
 - 207 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/(SICI)1098-1004(200002)15:2<207::AID-HUMU15>3.0.CO;2-F  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Glutaryl-CoA Dehydrogenase<br/>Haplotypes<br/>Humans<br/>Linkage Disequilibrium<br/>Mutation<br/>Oxidoreductases--deficiency<br/>Oxidoreductases Acting on CH-CH Group Donors<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic<br/>Polymorphism, Single-Stranded Conformational<br/>Spain