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Rare type I CBFβ/MYH11 fusion transcript in primary acute myeloid leukemia with inv(16)(p13.1q22): a case report
Inv(16)(p13.1q22) in acute myeloid leukemia (AML) is a common chromosomal abnormality. It leads to the core-binding factor ß-subunit (CBFβ)/smooth muscle myosin heavy chain 11 (MYH11) fusion gene. Different breakpoints were observed in the CBFβ gene at 16q22 and the MYH11 gene at 16p13.1. For this r...
Autores principales: | Zhang, Wenyi, Wang, Hainan, Zhang, Peilei, Li, Hongliang, Ma, Xiaoli, Liu, Hongxing |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Divulgação Científica
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8555453/ https://www.ncbi.nlm.nih.gov/pubmed/34730684 http://dx.doi.org/10.1590/1414-431X2021e11605 |
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