Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations

PURPOSE OF REVIEW: CCAAT enhancer binding protein A (CEBPA) gene mutation is one of the common genetic alterations in acute myeloid leukemia (AML), which can be associated with sporadic and familial AML. RECENT FINDINGS: Due to the recent advances in molecular testing and the prognostic role of CEBP...

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Detalles Bibliográficos
Autores principales: Yuan, Ji, He, Rong, Alkhateeb, Hassan B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484814/
https://www.ncbi.nlm.nih.gov/pubmed/37261703
http://dx.doi.org/10.1007/s11899-023-00699-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10484814/
https://www.ncbi.nlm.nih.gov/pubmed/37261703
http://dx.doi.org/10.1007/s11899-023-00699-3

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