Cancer risk associated with STK11/LKB1 germline mutations in Peutz–Jeghers syndrome patients: Results of an Italian multicenter study

Abstract Background Germline mutations in the STK11/LKB1 gene cause Peutz–Jeghers syndrome, an autosomal-dominantly inherited condition characterized by mucocutaneous pigmentation, hamartomatous gastrointestinal polyposis, and an increased risk for various malignancies. We here report the results of...

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Veröffentlicht in:Digestive and liver disease 2013-07, Vol.45 (7), p.606-611
Hauptverfasser: Resta, Nicoletta, Pierannunzio, Daniela, Lenato, Gennaro Mariano, Stella, Alessandro, Capocaccia, Riccardo, Bagnulo, Rosanna, Lastella, Patrizia, Susca, Francesco Claudio, Bozzao, Cristina, Loconte, Daria Carmela, Sabbà, Carlo, Urso, Emanuele, Sala, Paola, Fornasarig, Mara, Grammatico, Paola, Piepoli, Ada, Host, Cristina, Turchetti, Daniela, Viel, Alessandra, Memo, Luigi, Giunti, Laura, Stigliano, Vittoria, Varesco, Liliana, Bertario, Lucio, Genuardi, Maurizio, Lucci Cordisco, Emanuela, Tibiletti, Maria Grazia, Di Gregorio, Carmela, Andriulli, Angelo, Ponz de Leon, Maurizio
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Sprache:eng
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