alexa Detection of Glucose-6-Phosphate Dehydrogenase Deficiency in Heterozygous Saudi Female Neonates

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Detection of Glucose-6-Phosphate Dehydrogenase Deficiency in Heterozygous Saudi Female Neonates

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common genetic enzymopathy, affecting millions of people worldwide. Because G6PD deficiency is an X-linked condition, males may be either G6PD normal or G6PD deficient hemizygotes, whereas females may be, normal homozygotes, deficient homozygotes, or heterozygotes.

 

Citation: Jarullah J, AlJaouni S, Sharma MC, Bushra MSJ, Kamal MA (2012) Detection of Glucose-6-Phosphate Dehydrogenase Deficiency in Heterozygous Saudi Female Neonates. Enz Eng 1:105.

 

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