Glucose-6-phosphate dehydrogenase deficiency in the Han Chinese population: molecular characterization and genotype–phenotype association throughout an activity distribution
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Title
Glucose-6-phosphate dehydrogenase deficiency in the Han Chinese population: molecular characterization and genotype–phenotype association throughout an activity distribution
Authors
Keywords
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Journal
Scientific Reports
Volume 10, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-10-13
DOI
10.1038/s41598-020-74200-y
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Related references
Note: Only part of the references are listed.- Chinese newborn screening for the incidence of G6PD deficiency and variant of G6PD gene from 2013 to 2017
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- A trade off between catalytic activity and protein stability determines the clinical manifestations of glucose-6-phosphate dehydrogenase (G6PD) deficiency
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- Large Cohort Screening of G6PD Deficiency and the Mutational Spectrum in the Dongguan District in Southern China
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- Determination of optimal cutoff value to accurately identify glucose-6-phosphate dehydrogenase-deficient heterozygous female neonates
- (2013) Jing-Kun Miao et al. CLINICA CHIMICA ACTA
- Evaluation of the phenotypic test and genetic analysis in the detection of glucose-6-phosphate dehydrogenase deficiency
- (2013) Duangdao Nantakomol et al. MALARIA JOURNAL
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- (2011) Wei Ying Jiang et al. BIOCHEMICAL GENETICS
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- Glucose-6-phosphate dehydrogenase laboratory assay: How, when, and why?
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- Molecular characterization of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Tunisia
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