Brivet, M <br/><br/>
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.  [electronic resource] 

 -  Pediatric research  Feb 1983 
 - 157-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0031-3998 
<br/><br/><label>Standard No.: </label>10.1203/00006450-198302000-00015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Erythrocytes--metabolism<br/>Fanconi Syndrome--complications<br/>Female<br/>Galactose--metabolism<br/>Glucagon<br/>Glucose--metabolism<br/>Glycogen Storage Disease--complications<br/>Glycolysis<br/>Humans<br/>In Vitro Techniques<br/>Kidney--metabolism<br/>Liver--metabolism<br/>Liver Function Tests<br/>Oxidation-Reduction