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- W2015301581 abstract "Dear Editor, The increase of fetal hemoglobin (HbF), in adult life, is mainly due to large deletions within β-globin cluster in hereditary persistence of fetal hemoglobin (HPFH) and δβ- thalassemia or in some cases of nondeletional HPFH (nd- HPFH) by mutations in promoter region of γ-globin genes [1-3]. Several nd-HPFH mutations have been reported; most of these mutations occur in transcription factor binding sites, creating new factor binding motifs or disrupting the existing ones [2]. The Cretan type of nd- HPFH (Aγ-158 C>T) is characterized by slightly elevated HbF levels (2.9-5.1%) and normal hematological indices [4]. This mutation has resulted from two independent gene conversion events [4, 5]. It is identical to Gγ-globin gene XmnI polymorphism (Gγ-158 C>T) which also occurs in healthy individuals." @default.
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- W2015301581 date "2009-05-26" @default.
- W2015301581 modified "2023-09-23" @default.
- W2015301581 title "The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family" @default.
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- W2015301581 doi "https://doi.org/10.1007/s00277-009-0756-0" @default.
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