Letter to the Editor
Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases
Version of Record online: 11 DEC 2012
© 2012 John Wiley & Sons A/S
Pigment Cell & Melanoma Research
Volume 26, Issue 2, pages 278–279, March 2013
How to Cite
Aoude, L. G., Vajdic, C. M., Kricker, A., Armstrong, B. and Hayward, N. K. (2013), Prevalence of germline BAP1 mutation in a population-based sample of uveal melanoma cases. Pigment Cell & Melanoma Research, 26: 278–279. doi: 10.1111/pcmr.12046
- Issue online: 26 FEB 2013
- Version of Record online: 11 DEC 2012
- Accepted manuscript online: 22 NOV 2012 04:38AM EST
- National Health and medical Research Council of Australia
- Cancer Council, New South Wales
|pcmr12046-sup-0001-AppendixS1.docx||Word document||13K||Appendix S1. Methods.|
|pcmr12046-sup-0002-FigureS1.pdf||Word document||401K||Figure S1. Novel germline BAP1 mutations. In (a), the top left panel shows the c.1480_1481delga (P494fs) and the bottom left shows the wild type trace. The top right panel of (a) shows the C.1806g > c mutation with the wild type trace directly below it. (b) The truncating and missense mutations in relation to BAP1 protein domains. The figure is not drawn to scale.|
Table S1. BAP1 primer sequences.
Table S2. All germline BAP1 nucleotide changes observed in a sample of sporadic uveal melanoma cases.
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