Yokota, I <br/><br/>
The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.  [electronic resource] 

 -  Progress in clinical and biological research  1992 
 - 425-40 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0361-7742 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acyl-CoA Dehydrogenase<br/>Acyl-CoA Dehydrogenases--deficiency<br/>Adenine--physiology<br/>Alleles<br/>Base Sequence<br/>Biological Evolution<br/>Cells, Cultured<br/>Ethnicity--genetics<br/>Fibroblasts--physiology<br/>Genetic Variation--genetics<br/>Guanine--physiology<br/>Homozygote<br/>Humans<br/>Metabolism, Inborn Errors--enzymology<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Skin Physiological Phenomena<br/>Surveys and Questionnaires