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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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Cancer Res Treat
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Korean Cancer Association 2019
Θέματα:
Original Article
Διαθέσιμο Online: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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