A novel STK11 missense mutation (c.346G > T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history. [electronic resource]
- Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 08 2018
- 864-866 p. digital
Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
1878-3562
10.1016/j.dld.2018.05.020 doi
AMP-Activated Protein Kinase Kinases Adult China Gastrointestinal Hemorrhage--etiology Germ-Line Mutation Humans Intestinal Polyps--pathology Male Mutation, Missense Peutz-Jeghers Syndrome--diagnosis Protein Serine-Threonine Kinases--genetics