Scholte, H R <br/><br/>
Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.  [electronic resource] 

 -  Journal of inherited metabolic disease  1987 
 - 81-97 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1007/BF01812849  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Biotin--metabolism<br/>Brain--enzymology<br/>Carnitine--metabolism<br/>Cells, Cultured<br/>Child, Preschool<br/>Coenzyme A--metabolism<br/>Cytochrome-c Oxidase Deficiency<br/>Electron Transport Complex III--deficiency<br/>Female<br/>Fibroblasts--enzymology<br/>Humans<br/>Infant<br/>Male<br/>Metabolism, Inborn Errors--enzymology<br/>Mitochondria--enzymology<br/>Mitochondria, Liver--enzymology<br/>Mitochondria, Muscle--enzymology<br/>Mitochondrial ADP, ATP Translocases--deficiency<br/>NAD(P)H Dehydrogenase (Quinone)<br/>Oxidative Phosphorylation<br/>Quinone Reductases--deficiency