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OALib Journal期刊
ISSN: 2333-9721
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-  2019 

Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland

DOI: 10.4143/crt.2018.157

Keywords: Whole exome sequencing, Melanoma, Frameshift mutation

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Abstract:

Germline mutations within melanoma susceptibility genes are present only in minority of melanoma patients and it is expected that additional genes will be discovered with next generation sequence technology and whole-exome sequencing (WES)

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