Highly Sensitive Detection of IDH2 Mutations in Acute Myeloid Leukemia

Background: Acute myeloid leukemia is a heterogeneous hematological disease, characterized by karyotypic and molecular alterations. Mutations in IDH2 have a role in diagnosis and as a minimal residue disease marker. Often the variant allele frequency during follow up is less than 20%, which represen...

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Bibliografiske detaljer
Udgivet i:J Clin Med
Main Authors: Petiti, Jessica, Rosso, Valentina, Croce, Eleonora, Franceschi, Vanessa, Andreani, Giacomo, Dragani, Matteo, De Gobbi, Marco, Lunghi, Monia, Saglio, Giuseppe, Fava, Carmen, Lo Iacono, Marco, Cilloni, Daniela
Format: Artigo
Sprog:Inglês
Udgivet: MDPI 2020
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Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7019902/
https://ncbi.nlm.nih.gov/pubmed/31963812
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm9010271
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