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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Библиографические подробности
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Springer-Verlag 2008
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Original Article
Online-ссылка: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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