Exome sequencing revealed novel germline mutations in Chinese Peutz-Jeghers syndrome patients

Digestive Diseases and Sciences

Volumn 59, Issue 1, 2014, Pages 64-71

  Wang, Huan Huan ^a   Xie, Na Na ^a   Li, Qi Yuan ^b,c   Hu, Yi Qun ^a   Ren, Jian Lin ^a   Guleng, Bayasi ^a,b  

^a ZHONGSHAN HOSPITAL OF XIAMEN UNIVERSITY   (China)

^b XIAMEN UNIVERSITY   (China)

^c DANA FARBER CANCER INSTITUTE   (United States)

Author keywords

Candidate gene; Causative mutation; Peutz Jeghers syndrome; Whole exome sequencing

Indexed keywords

GENOMIC DNA; MICRORNA; PROTEIN KINASE LKB1;

ADULT; ARTICLE; CASE REPORT; CHILD; CHINESE; CONTROLLED STUDY; EXOME; FAMILY STUDY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC VARIABILITY; GENOME; GERM LINE; HUMAN; MALE; PEUTZ JEGHERS SYNDROME; PRIORITY JOURNAL; SCHOOL CHILD; WILD TYPE; YOUNG ADULT;

EID: 84893769960     PISSN: 01632116     EISSN: 15732568     Source Type: Journal    
DOI: 10.1007/s10620-013-2875-7     Document Type: Article

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