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FMN1 — PNP

Text-mined interactions from Literome

Anderson et al., Eur J Haematol 1989 (Thalassemia) : In 18 beta-thalassaemia families from the Ferrara area the incidence of an inherited low flavin mononucleotide (FMN) dependent pyridoxine phosphate (PNP) oxidase activity, a sensitive indicator of red-cell FMN deficiency, is higher in related members in these families than in the unrelated spouses and controls subjects without family history of thalassaemia
Anderson et al., Eur J Haematol 1987 (Glucosephosphate Dehydrogenase Deficiency...) : Unexpectedly, on the other hand, low FMN dependent PNP oxidase activity due to red-cell deficiency of FMN, confirmed by response to oral riboflavin, was found in the majority of subjects with G6PD deficiency, similar to that found in heterozygous beta-thalassaemia