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Some observations on glutathione instability and glucose-6-phosphate dehydrogenase deficiency in infants and children having anaemia and jaundice

โœ Scribed by K. Kalra; R. Prasad; N. N. Khanna; V. P. Mital; R. S. Dayal

Book ID
112905949
Publisher
Springer-Verlag
Year
1973
Tongue
English
Weight
407 KB
Volume
40
Category
Article
ISSN
0019-5456

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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