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GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY AND NEONATAL JAUNDICE IN CHINESE MALE INFANTS IN HONG KONG

โœ Scribed by Yue, PaulC.K.; Strickland, Maureen

Book ID
122769638
Publisher
The Lancet
Year
1965
Tongue
English
Weight
324 KB
Volume
285
Category
Article
ISSN
0140-6736

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Neonatal jaundice and molecular mutation
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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