Clinical profile in KMT2A-SEPT6-positive acute myeloid leukemia: Does it often co-occur with NRAS mutations?

BACKGROUND: The KMT2A-SEPT6 fusion gene is a relatively rare genetic event in leukemia. Its clinical characteristics and prognosis, especially the profile of co-occurring gene mutations remain unclear. METHODS: We retrospectively analyzed the characteristics of four cases carrying KMT2A-SEPT6 in our...

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Detalles Bibliográficos
Autores principales: Chen, Fang, Yang, Ying, Fu, Shuang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532577/
https://www.ncbi.nlm.nih.gov/pubmed/36213638
http://dx.doi.org/10.3389/fmed.2022.890959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9532577/
https://www.ncbi.nlm.nih.gov/pubmed/36213638
http://dx.doi.org/10.3389/fmed.2022.890959

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