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- W2014119773 abstract "The case history, laboratory findings and properties of the enzyme in a patient with hexokinase deficiency are reported. The mother had a haemolytic disorder of similar severity. In these cases the expression of the disease in both mother and son suggests a dominant mode of inheritance. This family further illustrates the necessity of taking the reticulocyte level into account when interpreting red cell enzyme levels." @default.
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- W2014119773 date "1980-12-01" @default.
- W2014119773 modified "2023-09-24" @default.
- W2014119773 title "Non-spherocytic Haemolytic Anaemia in Mother and Son Associated with Hexokinase Deficiency" @default.
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- W2014119773 doi "https://doi.org/10.1111/j.1365-2141.1980.tb06010.x" @default.
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