A novel STK11 missense mutation (c.346G > T) causing Peutz-Jeghers syndrome in a Chinese male with a negative family history.

Zhao, Zi-Ye

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