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  • Title: G-6PD "ankara". a new G-6PD variant with deficiency found in a Turkish family.
    Author: Kahn A, North ML, Messer J, Boivin P.
    Journal: Humangenetik; 1975; 27(3):247-50. PubMed ID: 1150245.
    Abstract:
    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-electrophoretic mobility (110% of normal), increased Ki NADPH with respect to NADP+, slightly biphasic pH curve, enzyme instability, in vivo and in vitro, decreased molecular specific activity (58% of normal).
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