Genotype-Phenotype Correlation of G6PD Mutations among Central Thai Children with G6PD Deficiency

Figure 1

Electropherogram of 12 G6PD mutations identified in this study; (a) G6PD Viangchan (c.871G>A, p.Val291Met), (b) G6PD Canton (c.1376G>T, p.Arg459Leu), (c) G6PD Kaiping (c.1388G>A, p.Arg463His), (d) G6PD Mahidol (c.487G>A, p.Gly163Ser), (e) G6PD Quing Yan (c.392G>T, p.Gly131Val), (f) G6PD Aures (c.143T>C, p.Ile48Thr), (g) G6PD Coimbra (c.592C>T, p.Arg198Cys), (h) G6PD Songklanagarind (c.196T>A, p.Phe66Ile), (i) G6PD Union (c.1360C>T, p.Arg454Cys), (j) G6PD Valladolid (c.406C>T, p.Arg136Cys), (k) G6PD Chinese-5 (c.1024C>T, p.Leu342Phe), and (l) G6PD Mediterranean (c.563C>T, p.Ser188Phe).