Cosson, M A <br/><br/>
Liver hepatoblastoma and multiple OXPHOS deficiency in the follow-up of a patient with methylmalonic aciduria.  [electronic resource] 

 -  Molecular genetics and metabolism   
 - 107-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1096-7206 
<br/><br/><label>Standard No.: </label>10.1016/j.ymgme.2008.06.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cells, Cultured<br/>Child<br/>Electron Transport<br/>Fatal Outcome<br/>Fibroblasts--enzymology<br/>Follow-Up Studies<br/>Hepatoblastoma--enzymology<br/>Humans<br/>Immunosuppressive Agents--adverse effects<br/>Kidney--enzymology<br/>Kidney Transplantation--adverse effects<br/>Lipid Metabolism, Inborn Errors--complications<br/>Male<br/>Methylmalonic Acid--metabolism<br/>Methylmalonyl-CoA Mutase--genetics<br/>Mutation