Incidence and molecular characterization of Glucose-6-Phosphate Dehydrogenase deficiency among neonates for newborn screening in Chaozhou, China

Summary Introduction Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is highly prevalent in southern China. The aim of this study is to assess the extent of this disease in Chinese neonates and determine its molecular characteristics using a novel molecular screening method. Methods A total of 2...

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Veröffentlicht in:	International journal of laboratory hematology 2015-06, Vol.37 (3), p.410-419
Hauptverfasser:	Yang, H., Wang, Q., Zheng, L., Zhan, X.-F., Lin, M., Lin, F., Tong, X., Luo, Z.-Y., Huang, Y., Yang, L.-Y.
Format:	Artikel
Sprache:	eng
Schlagworte:	Alleles China - epidemiology DNA Mutational Analysis Exons Female G6PD deficiency gene mutation Genetic Testing Genotype Glucosephosphate Dehydrogenase - genetics Glucosephosphate Dehydrogenase Deficiency - diagnosis Glucosephosphate Dehydrogenase Deficiency - epidemiology Glucosephosphate Dehydrogenase Deficiency - genetics high resolution melting analysis Humans Incidence Infant Infant, Newborn Male Mutation Neonatal Screening newborn screening Polymerase Chain Reaction - methods
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