High prevalence of germline <it>STK11 </it>mutations in Hungarian Peutz-Jeghers Syndrome patients

• Principais autores: Kasler Miklos (Autor), Solyom Szilvia (Autor), Kovacs Marietta (Autor), Papp Janos (Autor), Børresen-Dal (Autor), Olah Edith (Autor)
• Formato: Livro
• Publicado em: BMC, 2010-11-01T00:00:00Z.
• Assuntos: article
• Acesso em linha: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is a rare autosomal dominantly inherited disease characterized by gastrointestinal hamartomatous polyposis and mucocutaneous pigmentation. The genetic predisposition for PJS has been shown to be associate...