Genetic profiling of a rare condition: co-occurrence of albinism and multiple primary melanoma in a caucasian family

Multiple primary melanoma (MPM) is a rare condition, whose genetic basis has not yet been clarified. Only 8-12% of MPM are due to germline mutations of CDKN2A. However, other genes (POT1, BRCA1/2, MC1R, MGMT) have been demonstrated to be involved in predisposition to this pathology. To our knowledge...

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Dettagli Bibliografici
Pubblicato in:Oncotarget
Autori principali: De Summa, Simona, Guida, Michele, Tommasi, Stefania, Strippoli, Sabino, Pellegrini, Cristina, Concetta Fargnoli, Maria, Pilato, Brunella, Natalicchio, Iole, Guida, Gabriella, Pinto, Rosamaria
Natura: Artigo
Lingua:Inglês
Pubblicazione: Impact Journals LLC 2016
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Research Paper
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5444700/
https://ncbi.nlm.nih.gov/pubmed/27776349
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.12777
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