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δ-aminolevulinate dehydrase: a new genetic polymorphism in man

✍ Scribed by G. BATTISTUZZI; R. PETRUCCI; L. SILVAGNI; F. R. URBANI; S. CAIOLA

Book ID
115248898
Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
377 KB
Volume
45
Category
Article
ISSN
0003-4800

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Polymorphism of red cell glyoxalase I (E.C.: 4.4.1.5). A new genetic marker in man
✍ J. Kömpf; S. Bissbort; S. Gussmann; H. Ritter 📂 Article 📅 1975 🏛 Springer 🌐 English ⚖ 151 KB

The polymorphism of glyoxalase I was investigated in 169 mother-child combinations from southwestern Germany. Glyoxalase I (GLO) has 3 common phenotypes: GLO 1, GLO 2-1, and GLO 2. The results are in good agreement with the formal hypothesis: Two alleles GLO1 and GLO2 at an autosomal locus. The GLO1