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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Detalhes bibliográficos
Publicado no:Cancer Res Treat
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Korean Cancer Association 2019
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6333986/
https://ncbi.nlm.nih.gov/pubmed/29764119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4143/crt.2018.157
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