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

PURPOSE: 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). MATERIALS AND METHODS: Herein we performed WES on...

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Detalles Bibliográficos
Autores principales: Dębniak, Tadeusz, Scott, Rodney J, Lea, Rodney A, Górski, Bohdan, Masojć, Bartłomiej, Cybulski, Cezary, Kram, Andrzej, Maleszka, Romuald, Gromowski, Tomasz, Paszkowska-Szczur, Katarzyna, Kashyap, Aniruddh, Lener, Marcin R., Malińska, Karolina, Rogoża, Emilia, Murawa, Dawid, Rudnicka, Helena, Deptuła, Jakub, Lubiński, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Cancer Association 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333986/
https://www.ncbi.nlm.nih.gov/pubmed/29764119
http://dx.doi.org/10.4143/crt.2018.157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6333986/
https://www.ncbi.nlm.nih.gov/pubmed/29764119
http://dx.doi.org/10.4143/crt.2018.157

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