The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter

Nondeletional hereditary persistence of fetal hemoglobin (nd-HPFH), a rare hereditary condition resulting in elevated levels of fetal hemoglobin (Hb F) in adults, is associated with promoter mutations in the human fetal globin (HBG1 and HBG2) genes. In this paper, we report a novel type of nd-HPFH d...

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Main Authors: Chassanidis, Christos, Kalamaras, Angelos, Phylactides, Marios, Pourfarzad, Farzin, Likousi, Sophia, Maroulis, Vassilis, Papadakis, Manoussos N., Vamvakopoulos, Nikolaos K., Aleporou-Marinou, Vassiliki, Patrinos, George P., Kollia, Panagoula
Format: Artigo
Jezik:Inglês
Izdano: Springer-Verlag 2008
Teme:
Original Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2690858/
https://ncbi.nlm.nih.gov/pubmed/19050890
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00277-008-0643-0
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