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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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| Veröffentlicht in: | Ophthalmology |
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| Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | 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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