A new G-6PD varient with enzyme deficiency is described in a 7-month-old Turkish boy without any hemolytic manifestation, except neonatal hyperbilirubinemia. The main characteristics of this variant were the following: Severe enzyme deficiency in erythrocytes (8% of normal), fast starch-gel-electrop
Characterization of G6PD deficiency in southern Croatia: description of a new variant, G6PD Split
✍ Scribed by Marin Barišić; Jelena Korać; Ivana Pavlinac; Vjekoslav Krželj; Eugenija Marušić; Tom Vulliamy; Janoš Terzić
- Publisher
- Nature Publishing Group
- Year
- 2005
- Tongue
- English
- Weight
- 153 KB
- Volume
- 50
- Category
- Article
- ISSN
- 1435-232X
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