Next-Generation Sequencing of DDX41 in Myeloid Neoplasms Leads to Increased Detection of Germline Alterations

Previously considered rare, inherited hematologic malignancies are increasingly identified. Germline mutations in the RNA helicase DDX41 predispose to increased lifetime risks of myeloid neoplasms with disease often occurring later in life which presents challenges for germline recognition. To impro...

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Dades bibliogràfiques
Publicat a:Front Oncol
Autors principals: Bannon, Sarah A., Routbort, Mark J., Montalban-Bravo, Guillermo, Mehta, Rohtesh S., Jelloul, Fatima Zahra, Takahashi, Koichi, Daver, Naval, Oran, Betul, Pemmaraju, Naveen, Borthakur, Gautam, Naqvi, Kiran, Issa, Ghayas, Sasaki, Koji, Alvarado, Yesid, Kadia, Tapan M., Konopleva, Marina, Shamanna, Rashmi Kanagal, Khoury, Joseph D., Ravandi, Farhad, Champlin, Richard, Kantarjian, Hagop M., Bhalla, Kapil, Garcia-Manero, Guillermo, Patel, Keyur P., DiNardo, Courtney D.
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Oncology
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7878971/
https://ncbi.nlm.nih.gov/pubmed/33585199
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fonc.2020.582213
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