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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Spremljeno u:
Bibliografski detalji
Izdano u:Cancer Res Treat
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Korean Cancer Association 2019
Teme:
Original Article
Online pristup: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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