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
β¦ LIBER β¦
Three mutations analysis of glucose-6-phosphate dehydrogenase deficiency in neonates in South-west China
β Scribed by CHUN DENG; CHUN-BAO GUO; YOU-HUA XU; BING DENG; JIA-LIN YU
- Book ID
- 108971316
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 92 KB
- Volume
- 49
- Category
- Article
- ISSN
- 1328-8067
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