Whole exome sequencing identifies candidate genes associated with hereditary predisposition to uveal melanoma

OBJECTIVE: The aim of this study was to identify susceptibility genes associated with hereditary predisposition to uveal melanoma (UM) in patients with no detectable germline BAP1 alterations. DESIGN: Retrospective case series from academic referral centers. PARTICIPANTS: Cohort of 154 UM patients w...

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Bibliografske podrobnosti
izdano v:Ophthalmology
Main Authors: Abdel-Rahman, Mohamed H., Sample, Klarke M., Pilarski, Robert, Walsh, Tom, Grosel, Timothy, Kinnamon, Daniel, Boru, Getachew, Massengill, James B., Schoenfield, Lynn, Kelly, Ben, Gordon, David, Johansson, Peter, DeBenedictis, Meghan J., Singh, Arun, Casadei, Silvia, Davidorf, Frederick H., White, Peter, Stacey, Andrew W., Scarth, James, Fewings, Ellie, Tischkowitz, Marc, King, Mary-Claire, Hayward, Nicholas K., Cebulla, Colleen M.
Format: Artigo
Jezik:Inglês
Izdano: 2019
Teme:
Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7183432/
https://ncbi.nlm.nih.gov/pubmed/32081490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ophtha.2019.11.009
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