Katarzyna Zak-Jasinska

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Dear Editor, We present a case of a 6-year-old boy of Polish origin who was diagnosed with glucose-6-phosphate dehydrogenase (G6PD) deficiency due to Seoul mutation. The patient was born prematurely in the 36th week of gestation. There was no history of any hematological disorders in parental families. At birth, it was noted that the patient presented(More)
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