Cytogenetic and FMS-Like Tyrosine Kinase 3 Mutation Analyses in Acute Promyelocytic Leukemia Patients

Background: The secondary genetic changes other than the promyelocytic leukemia-retinoic acid receptor (PML-RARA) fusion gene may contribute to the acute promyelocytic leukemogenesis. Chromosomal alterations and mutation of FLT3 (FMS-like tyrosine kinase 3) tyrosine kinase receptor are the frequent...

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Detalhes bibliográficos
Main Authors: Yaghmaie, Marjan, Alimoghaddam, Kamran, Mozdarani, Hossein, Ghavamzadeh, Ardeshir, Hajhashemi, Marjan, Aznab, Mozaffar, Ghaffari, Seyed H.
Formato: Artigo
Idioma:Inglês
Publicado em: Pasteur Institute of Iran 2012
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3614257/
https://ncbi.nlm.nih.gov/pubmed/22562027
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6091/IBJ.961.2012
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