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Glucose-6-phosphate dehydrogenase deficiency and colour-vision studies in Indian Muslims

โœ Scribed by S. M. A. Hakim; A. J. Baxi; V. Balakrishnan; K. V. Kulkarni; S. S. Rao; H. I. Jhala

Publisher
Springer
Year
1972
Tongue
English
Weight
149 KB
Volume
15
Category
Article
ISSN
0340-6717

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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