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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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| Publicado no: | SAGE Open Med Case Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5758965/ https://ncbi.nlm.nih.gov/pubmed/29326822 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2050313X17750334 |
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