Brivet, M <br/><br/>
[Hereditary abnormalities of galactose metabolism: diagnosis and biochemical supervision (author's transl)].  [electronic resource] 

 -  Annales de biologie clinique  1979 
 - 259-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>0003-3898 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Biological Assay--methods<br/>Carbohydrate Epimerases--deficiency<br/>Carbohydrate Metabolism, Inborn Errors--diagnosis<br/>Chromatography, Paper<br/>Erythrocytes--enzymology<br/>Escherichia coli--enzymology<br/>Female<br/>Galactokinase--deficiency<br/>Galactose--metabolism<br/>Galactosemias<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Infant, Newborn<br/>Infant, Newborn, Diseases--diagnosis<br/>Nucleotidyltransferases--deficiency<br/>Pregnancy<br/>Prenatal Diagnosis<br/>UDPglucose 4-Epimerase--deficiency<br/>UDPglucose-Hexose-1-Phosphate Uridylyltransferase--blood