Common Genetic Variations in Patched1 (PTCH1) Gene and Risk of Hirschsprung Disease in the Han Chinese Population

PLoS ONE

Volumn 8, Issue 9, 2013, Pages

  Wang, Yang ^a,b,c   Wang, Jun ^a,b,c   Pan, Weihua ^a,b,c   Zhou, Ying ^a,b,c   Xiao, Yongtao ^a,b,c   Zhou, Kejun ^a,b,c   Wen, Jie ^a,b,c   Yu, Tingxi ^a,b,c   Cai, Wei ^a,b,c  

^a SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

^b Shanghai Key Laboratory of Pediatric Gastroenterology and Nutrition   (China)

^c Shanghai Institute for Pediatric Research   (China)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN PATCHED 1;

ALLELE; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC MARKER; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; MAJOR CLINICAL STUDY; MALE; PATCHED1 GENE; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHINA; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HAPLOTYPES; HIRSCHSPRUNG DISEASE; HUMANS; INFANT; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, CELL SURFACE; RISK FACTORS;

EID: 84884472739     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0075407     Document Type: Article

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