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

• Main Authors: Singh Lalji (Author), Mohankrishna P (Author), Rao G (Author), Reddy D (Author), Thakur Nikita (Author), Chandak Giriraj R (Author)
• Format: Knjiga
• Izdano: BMC, 2006-09-01T00:00:00Z.
• Teme: article
• Online dostop: 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>...