Author:
Maciejewski-Duval Anna,Meuris Floriane,Bignon Alexandre,Aknin Marie-Laure,Balabanian Karl,Faivre Laurence,Pasquet Marlène,Barlogis Vincent,Fieschi Claire,Bellanné-Chantelot Christine,Donadieu Jean,Schlecht-Louf Géraldine,Marin-Esteban Viviana,Bachelerie Francoise
Funder
F.B.
K.B.
G.S.L.
Laboratoire d'Excellence en Recherche sur le Médicament et l'Innovation Thérapeutique
Institut National de la Santé et de la Recherche Médicale
CEREDIH
French National Reference Center for Primary Immune Deficiencies
Subject
Cell Biology,Immunology,Immunology and Allergy
Reference71 articles.
1. Dendritic cell, monocyte, B and NK lymphoid deficiency defines the lost lineages of a new GATA-2 dependent myelodysplastic syndrome;Bigley;Haematologica,2011
2. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency;Dickinson;Blood,2011
3. Deaf-mutism, lymphedema of the lower limbs and hematological abnormalities (acute leukemia, cytopenia) with autosomal dominant transmission [in French];Emberger;J. Genet. Hum.,1979
4. GATA2 deficiency-associated bone marrow disorder differs from idiopathic aplastic anemia;Ganapathi;Blood,2015
5. Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia;Hahn;Nat. Genet.,2011
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