Haworth, J C <br/><br/>
Phenotypic variability in glutaric aciduria type I: Report of fourteen cases in five Canadian Indian kindreds.  [electronic resource] 

 -  The Journal of pediatrics  Jan 1991 
 - 52-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-3476 
<br/><br/><label>Standard No.: </label>10.1016/s0022-3476(05)81843-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Amino Acid Metabolism, Inborn Errors--genetics<br/>Canada<br/>Child<br/>Child, Preschool<br/>Female<br/>Glutarates--metabolism<br/>Glutaryl-CoA Dehydrogenase<br/>Humans<br/>Indians, North American--genetics<br/>Infant<br/>Male<br/>Oxidoreductases--deficiency<br/>Oxidoreductases Acting on CH-CH Group Donors<br/>Phenotype