Electrophoretic abnormality of galactose-1-phosphate uridyl transferase in galactosemia
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference9 articles.
1. A NEW GENETIC ABNORMALITY RESULTING IN GALACTOSE-1-PHOSPHATE URIDYLTRANSFERASE DEFICIENCY
2. Clinical variants of galactosemia
3. Electrophoretic Variation of Galactose-1-Phosphate Uridyltransferase
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1. Diseases Associated with Primary Abnormalities in Carbohydrate Metabolism;Swaiman's Pediatric Neurology;2012
2. An unusual form of galactosemia: Studies on erythrocytes and hair roots;Clinical Genetics;2008-06-28
3. Prenatal diagnosis of galactosaemia in six pregnancies' possible complications with rare alleles of the galactose 1-phosphate uridyl transferase locus;Clinical Genetics;2008-04-23
4. Galactose-1-phosphate accumulation by a Duarte-transferase deficiency double heterozygote;Clinical Genetics;2008-04-23
5. Galactosemia: screening and diagnosis;Clinical Biochemistry;1991-08
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