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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Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2008
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690858/
https://www.ncbi.nlm.nih.gov/pubmed/19050890
http://dx.doi.org/10.1007/s00277-008-0643-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2690858/
https://www.ncbi.nlm.nih.gov/pubmed/19050890
http://dx.doi.org/10.1007/s00277-008-0643-0

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