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Phototherapy in newborn infants with glucose-6-phosphate dehydrogenase deficiency

โœ Scribed by Arthur E. Kopelman; John L. Ey; Hahng Lee

Book ID
119457096
Publisher
Elsevier Science
Year
1978
Tongue
English
Weight
258 KB
Volume
93
Category
Article
ISSN
1097-6833

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โœ Huang, Ching-Shan; Hung, Kun-Long; Huang, May-Jen; Li, Yi-Ching; Liu, Te-Hui; Ta ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 553 KB

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