Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency. [Blood. 2011] Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome
Titolo: | GATA2 finds its macrophage niche. |
Autore/i: | FRANCO MIGLIACCIO, ANNA RITA; Bieker, Jj |
Autore/i Unibo: | |
Anno: | 2011 |
Rivista: | |
Digital Object Identifier (DOI): | http://dx.doi.org/10.1182/blood-2011-06-362772 |
Abstract: | Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency. [Blood. 2011] Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome |
Data stato definitivo: | 2015-10-27T09:47:56Z |
Appare nelle tipologie: | 1.01 Articolo in rivista |
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