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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Bibliografske podrobnosti
izdano v:Front Oncol
Main Authors: 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
Jezik:Inglês
Izdano: Frontiers Media S.A. 2021
Teme:
Oncology
Online dostop: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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