High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia

Marlène Pasquet; Christine Bellanné-Chantelot; Suzanne Tavitian; Naïs Prade; Blandine Beaupain; Olivier LaRochelle; Arnaud Petit; Pierre Rohrlich; Christophe Ferrand; Eric Van Den Neste; Hélène A. Poirel; Thierry Lamy; Marie Ouachée-Chardin; Véronique Mansat-De Mas; Jill Corre; Christian Récher; Geneviève Plat; Françoise Bachelerie; Jean Donadieu; Eric Delabesse; Donadieu; Donadieu; Owen; Song; Smith; Kirwan; Hahn; Ostergaard; Bödör; Kazenwadel; Holme; Dickinson; Hsu; Emberger; Mansour; Bellanné-Chantelot; Doncker; Balabanian; Zhang; Yan; Minelli; Balabanian; Balabanian; Jaeger

10.1182/blood-2012-08-447367

High frequency of GATA2 mutations in patients with mild chronic neutropenia evolving to MonoMac syndrome, myelodysplasia, and acute myeloid leukemia

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Last time updated on 12/3/2019

This paper was published in Crossref.

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