Rare missense variants in POT1 predispose to familial cutaneous malignant melanoma

Although CDKN2A is the most frequent high-risk melanoma susceptibility gene, the underlying genetic factors for most melanoma-prone families remain unknown. Using whole exome sequencing, we identified a rare variant that arose as a founder mutation in the telomere shelterin POT1 gene (g.7:124493086...

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Detalhes bibliográficos
Main Authors: Shi, Jianxin, Yang, Xiaohong R., Ballew, Bari, Rotunno, Melissa, Calista, Donato, Fargnoli, Maria Concetta, Ghiorzo, Paola, Paillerets, Brigitte Bressac-de, Nagore, Eduardo, Avril, Marie Francoise, Caporaso, Neil E., McMaster, Mary L., Cullen, Michael, Wang, Zhaoming, Zhang, Xijun, Bruno, William, Pastorino, Lorenza, Queirolo, Paola, Banuls-Roca, Jose, Garcia-Casado, Zaida, Vaysse, Amaury, Mohamdi, Hamida, Riazalhosseini, Yasser, Foglio, Mario, Jouenne, Fanélie, Hua, Xing, Hyland, Paula L., Yin, Jinhu, Vallabhaneni, Haritha, Chai, Weihang, Minghetti, Paola, Pellegrini, Cristina, Ravichandran, Sarangan, Eggermont, Alexander, Lathrop, Mark, Peris, Ketty, Scarra, Giovanna Bianchi, Landi, Giorgio, Savage, Sharon A., Sampson, Joshua N., He, Ji, Yeager, Meredith, Goldin, Lynn R., Demenais, Florence, Chanock, Stephen J., Tucker, Margaret A., Goldstein, Alisa M., Liu, Yie, Landi, Maria Teresa
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4056593/
https://ncbi.nlm.nih.gov/pubmed/24686846
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2941
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