Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis

Fuente: Wiley Open Access

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Bibliographic Details
Main Authors:	Laureano J. Kamiya, Serena Barozzi, Federica Isidori, Daiana Ganiewich, Geraldine De Luca, Valeria Bozzi, Rosana F. Marta, Federica Melazzini, Tommaso Pippucci, Paula G. Heller, Ana C. Glembotsky, Alessandro Pecci
Format:	Artículo Open Access
Published:	Wiley 2024
Subjects:	British Journal of Haematology
Online Access:	Acceder al recurso
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