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
GATA2 finds its macrophage niche / FRANCO MIGLIACCIO, ANNA RITA; Bieker, Jj. - In: BLOOD. - ISSN 0006-4971. - STAMPA. - 118:(2011), pp. 2647-2649. [10.1182/blood-2011-06-362772]
GATA2 finds its macrophage niche.
FRANCO MIGLIACCIO, ANNA RITA;
2011
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) syndromeFile in questo prodotto:
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