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Incomplete Dosage Compensation for Glucose-6-phosphate Dehydrogenase in Human Embryos and Newborns

โœ Scribed by STEELE, MARK W.

Book ID
109674609
Publisher
Nature Publishing Group
Year
1970
Tongue
English
Weight
403 KB
Volume
227
Category
Article
ISSN
0028-0836

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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