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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Publicado no: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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha: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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