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Erythrocyte acetylcholinesterase and glucose-6-phosphate dehydrogenase in newborn infants of low birth weight

โœ Scribed by Fritz Herz; Eugene Kaplan; Elsie S. Scheye


Book ID
115819721
Publisher
Elsevier Science
Year
1973
Tongue
English
Weight
466 KB
Volume
46
Category
Article
ISSN
0009-8981

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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