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
FRANCO MIGLIACCIO, A.R., Bieker, J.j. (2011). GATA2 finds its macrophage niche. BLOOD, 118, 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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