Acute myeloid leukemia with KMT2A-SEPT5 translocation: A case report and review of the literature

Chromosomal rearrangement involving the KMT2A gene is one of the most common genetic alteration in acute myeloid leukemia. A total of 135 different KMT2A rearrangements have been identified, where 94 translocation partner genes are now characterized at the molecular level. Of these 94 translocation...

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Detalles Bibliográficos
Autores principales: Elzamly, Shaimaa, Chavali, Santosh, Tonk, Vijay, Tonk, Sahil, Gaur, Sumit, Tarango, Darlene, Torabi, Alireza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758965/
https://www.ncbi.nlm.nih.gov/pubmed/29326822
http://dx.doi.org/10.1177/2050313X17750334

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758965/
https://www.ncbi.nlm.nih.gov/pubmed/29326822
http://dx.doi.org/10.1177/2050313X17750334

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