A Genome-Wide association study identifies potential susceptibility loci for hirschsprung disease

PLoS ONE

Volumn 9, Issue 10, 2014, Pages

  Kim, Jeong Hyun ^a   Cheong, Hyun Sub ^b   Sul, Jae Hoon ^c   Seo, Jeong Meen ^d   Kim, Dae Yeon ^e   Oh, Jung Tak ^f   Park, Kwi Won ^g   Kim, Hyun Young ^g   Jung, Soo Min ^d   Jung, Kyuwhan ^h   Cho, Min Jeng ⁱ   Bae, Joon Seol ^d   Shin, Hyoung Doo ^a,b  

^a Sogang University   (South Korea)

^b SNP Genetics Inc   (South Korea)

^c Engineering IV   (United States)

^d Samsung Medical Center   (South Korea)

^e University of Ulsan College of Medicine   (South Korea)

^f Yonsei University College of Medicine   (South Korea)

^g Seoul National University Children's Hospital   (South Korea)

^h Seoul National University Bundang Hospital   (South Korea)

ⁱ Konkuk University Hospital   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CONTROLLED STUDY; CSGALNACT2 GENE; EPIGENETICS; FEMALE; GENE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENETIC HETEROGENEITY; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; HIRSCHSPRUNG DISEASE; HUMAN; INTESTINE INNERVATION; MAJOR CLINICAL STUDY; MALE; NRG1 GENE; PATHOGENESIS; PRINCIPAL COMPONENT ANALYSIS; RASGEF1A GENE; RET GENE; SINGLE NUCLEOTIDE POLYMORPHISM; GENE LINKAGE DISEQUILIBRIUM; GENETIC PREDISPOSITION; GENETICS; HUMAN CHROMOSOME;

CHROMOSOMES, HUMAN; FEMALE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HIRSCHSPRUNG DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84907973558     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0110292     Document Type: Article

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