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- W2094393310 abstract "The type I hexokinase (HK-I) deficiency is a rare red cell enzymopathy associated with hereditary nonspherocytic hemolytic anemia. To date, only 16 affected families have been reported.[1][1] We report here prenatal diagnosis and molecular analysis of a Japanese family of HK deficiency. The proband'" @default.
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- W2094393310 date "2002-09-01" @default.
- W2094393310 modified "2023-09-27" @default.
- W2094393310 title "Homozygous intragenic deletion of type I hexokinase gene causes lethal hemolytic anemia of the affected fetus" @default.
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- W2094393310 doi "https://doi.org/10.1182/blood-2002-05-1599" @default.
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