A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients

A novel mutation in STK11 gene is associated with Peutz-Jeghers Syndrome in Chinese patients

<p>Abstract</p> <p>Background</p> <p>Peutz-Jeghers syndrome (PJS) is caused by mutations in the tumor suppressor gene, STK11, and is characterized by gastrointestinal hamartomas, melanin spots on the lips, and an increased risk of developing cancer.</p> <p>M...

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Bibliographic Details
Main Authors: Wang Zhiqing, Chen Yulan, Wu Baoping, Zheng Haoxuan, He Jiman, Jiang Bo
Format: Article
Language:English
Published: BMC 2011-12-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/12/161

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