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Incidence and causes of sepsis in glucose-6-phosphate dehydrogenase-deficient newborn infants

โœ Scribed by Yousef K. Abu-Osba; Ahmad A. Mallouh; Richard W. Hann

Book ID
119463484
Publisher
Elsevier Science
Year
1989
Tongue
English
Weight
452 KB
Volume
114
Category
Article
ISSN
1097-6833

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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