Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs

Hereditary persistence of fetal hemoglobin deletion type-2 (HPFH-2) and Sicilian-δβ-thalassemia are conditions described as large deletions of the human β-like globin cluster, with absent β-globin chains and a compensatory variable increase in γ-globin. HPFH, in general, may be distinguished from DB...

Description complète

Enregistré dans:
Détails bibliographiques
Publié dans:Exp Biol Med (Maywood)
Auteurs principaux: Fornari, Thais A, Lanaro, Carolina, Albuquerque, Dulcinéia M, Ferreira, Regiane, Costa, Fernando F
Format: Artigo
Langue:Inglês
Publié: SAGE Publications 2016
Sujets:
Original Research
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC5384494/
https://ncbi.nlm.nih.gov/pubmed/27591578
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1535370216668052
Tags: Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!

Documents similaires