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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Vydáno v:Cancer Res Treat
Hlavní autoři: 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
Médium: Artigo
Jazyk:Inglês
Vydáno: Korean Cancer Association 2019
Témata:
Original Article
On-line přístup: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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