High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
Claude Preudhomme(Centre National de la Recherche Scientifique), Pierre Fenaux(Hôpital Avicenne), Delphine Warot-Loze(Inserm), Elizabeth Macintyre(Université Paris Cité), Jean Luc Laı̈(Inserm), Nalthalie Grardel-Duflos(Inserm), Alain Cosson(Inserm), Richard Garand(Inserm), Nicole Dastugue(Inserm), Claude Denis(Inserm), F Bauters(Centre Hospitalier Universitaire de Lille), Jean Pierre Kerckaert(Inserm), Christophe Roumier(Université de Lille)
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