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. 2015 Sep 10;10(9):e0138038. doi: 10.1371/journal.pone.0138038

Correction: Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency at the China-Myanmar Border

Qing Li, Fang Yang, Rong Liu, Lan Luo, Yuling Yang, Lu Zhang, Huaie Liu, Wen Zhang, Zhixiang Fan, Zhaoqing Yang, Liwang Cui, Yongshu He
PMCID: PMC4565689  PMID: 26355741

There are errors in the Results section of this article. In fifth sentence of the “Identification of G6PD mutations” subsection, 9.7% should be 89.7%. The correct sentence is: Of these 87 cases, the Mahidol 487G>A type was the most predominant, occurring in 89.7% (78/87) of the subjects.

In the eighth sentence of the same subsection, 58.0% should be 48%. The correct sentence is: In addition, the silent mutation 1311C>T and the intron 11 mutation IVS11nt93T>C co-occurred in 48% (95/198) of the tested individuals (Table 2).

Table 2. Prevalence [n (%)] of G6PD variants in 198 unrelated G6PD-deficient participants # .

Mutations Amino Acid Substitution Total (n = 198) Female (n = 147) Male (n = 51) P *
Homozygous Heterozygous
Nonsynonymous mutations
Chinese 4 392G>T G131V 1 (0.5%) 0 1 (0.7%) 0
Mahidol 487G>A G163S 76 (38.4%) 5 (3.4%) 52 (35.4%) 19 (37.3%) 0.870
Viangchan 871G>A V291M 1 (0.5%) 0 1 (0.7%) 0
Canton 1376G>T R459L 1 (0.5%) 0 1 (0.7%) 0
Kaiping 1388G>A R463H 6 (3.0%) 1 (0.7%) 3 (2.0%) 2 (3.9%) 0.000
Mahidol/Viangchan G163S/V291M 1 (0.5%) 0 1 (0.7%) 0
Mahidol/Kaiping G163S/R463H 1 (0.5%) 0 1 (0.7%) 0
Synonymous mutations
1311C >T/93 T>C** Silent mutations 95 (48.0%) 9 (6.1%) 74 (50.3%) 12 (23.5%) 0.000
Unknown 42 (21.2%) 24 (16.3%) 18 (35.3%)

# The mutations Gaohe 95 A >G (H32R), Coimbra 592 C >T (R198C), Chinese 5 1024C >T (L342F), and Union 1360 C>T (R454C) were genotyped and not found in this study population.

*P value shows the differences in the prevalence of major G6PD deficiency variants between males and females compared using the Fisher’s exact test (two-tailed).

** 24 and 2 of these double silent mutations co-occurred in females heterozygous for the Mahidol and Kaiping mutations, respectively.

In addition, there is an error in Table 2: The value 18(35.3%) should not appear in the “Heterozygous” column but in the “Male (n = 51)” column. Please see the correct Table 2 here.

Reference


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