A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family

A novel mutation (c.855delG) in STK11 gene is associated with Peutz-Jeghers syndrome in a Chinese family

Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Digestive and Liver Disease - Volume 50, Issue 3, March 2018, Pages 312-314

Zi-Ye Zhao, Yu-Liang Jiang, Bai-Rong Li, En-Da Yu, Shou-Bin Ning,