Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation

被引：12
作者：
Zhao, Hong-Mei [1 ]
Yang, Yong-Jia [2 ]
Duan, Jia-Qi [1 ]
Ouyang, Hong-Juan [1 ]
Liu, Li [1 ]
Yi, Li-Chun [1 ]
Xiao, Zheng-Hui [1 ]
Zheng, Yu [1 ]
Peng, Lv [1 ]
Attard, Thomas M. [3 ]
Li, Ding-You [3 ]
You, Jie-Yu [1 ]
机构：
[1] Hunan Childrens Hosp, Dept Gastroenterol, 86 Ziyuan Rd, Changsha 410007, Hunan, Peoples R China
[2] Hunan Childrens Hosp, Inst Pediat Res, Changsha, Hunan, Peoples R China
[3] Childrens Mercy Kansas City, Div Gastroenterol, Kansas City, MI USA
来源：
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION | 2019年 / 68卷 / 02期
基金：
中国国家自然科学基金;
关键词：
children; de novo mutation; hereditary cancer; Peutz-Jeghers syndrome; polyposis syndrome; STK11; CHINESE PATIENTS; INCREASED RISK; CANCER; LOCALIZATION; POLYPECTOMY;
D O I：
10.1097/MPG.0000000000002166
中图分类号：
R57 [消化系及腹部疾病];
学科分类号：
摘要：
Supplemental Digital Content is available in the text
引用
收藏
页码：199 / 206
页数：8
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