A novel mutation in <it>STK11 </it>gene is associated with Peutz-Jeghers Syndrome in Indian patients

• Autori principali: Singh Lalji (Autore), Mohankrishna P (Autore), Rao G (Autore), Reddy D (Autore), Thakur Nikita (Autore), Chandak Giriraj R (Autore)
• Natura: Libro
• Pubblicazione: BMC, 2006-09-01T00:00:00Z.
• Soggetti: article
• Accesso online: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is a rare multi-organ cancer syndrome and understanding its genetic basis may help comprehend the molecular mechanism of familial cancer. A number of germ line mutations in the <it>STK11 </it>...