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Glucose-6-phosphate dehydrogenase deficiency and sulfadimidin acetylation phenotypes in Egyptian oases

โœ Scribed by Laila Hussein; Gamal Yamamah; Adly Saleh

Publisher
Springer
Year
1992
Tongue
English
Weight
451 KB
Volume
30
Category
Article
ISSN
0006-2928

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Molecular mutations of the giucose-Cphosphate dehydrogenase (G6PD) gene and clinical manifestations of neonatal jaundice in 112 male and 50 female Chinese neonates with G6PD deficiency were studied. In the 112 males, the nucleotide (nt) 1376 (G-T) mutation was the dominant type (50.0%), followed by