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Volumn 10, Issue 9, 2015, Pages

Low-frequency IL23R coding variant associated with Crohn's disease susceptibility in Japanese subjects identified by personal genomics analysis

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; BIOTINYLATION; CASE CONTROL STUDY; CONTROLLED STUDY; CROHN DISEASE; DISEASE PREDISPOSITION; FEMALE; FOLLOW UP; GENE; GENE FREQUENCY; GENETIC LINKAGE; GENETIC PREDISPOSITION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; HAPLOTYPE; HIGH THROUGHPUT SEQUENCING; HOMOZYGOSITY; HUMAN; IL23R GENE; MAJOR CLINICAL STUDY; MALE; NEXT GENERATION SEQUENCING; POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM; COMPARATIVE STUDY; GENETICS; GENOMICS; MIDDLE AGED; PATHOLOGY; PEDIGREE; PERSONALIZED MEDICINE; YOUNG ADULT;

EID: 84945539282     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0137801     Document Type: Article
Times cited : (8)

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