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Volumn 15, Issue 1, 2014, Pages

Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner

Author keywords

Atrial fibrillation; Expression QTL mapping; Genome wide association study; Trans ethnic mapping

Indexed keywords

ADULT; AGED; ALLELE; ANCESTRY GROUP; ARTICLE; BRITISH CITIZEN; CARDIOVASCULAR DISEASE; CHROMOSOME 16Q; CONTROLLED STUDY; ENGLAND; EXON; FEMALE; GENE; GENE EXPRESSION REGULATION; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE MAPPING; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; GENOME-WIDE ASSOCIATION STUDY; HUMAN; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; SINGLE NUCLEOTIDE POLYMORPHISM; SOUTH AFRICA; VERY ELDERLY; ZFHX3 GENE; ADOLESCENT; ATRIAL FIBRILLATION; CHROMOSOME 16; GENE FREQUENCY; GENETIC PREDISPOSITION; GENETICS; METABOLISM; MIDDLE AGED; MUCOCUTANEOUS LYMPH NODE SYNDROME; QUANTITATIVE TRAIT LOCUS; TRANSCRIPTION INITIATION SITE; YOUNG ADULT;

EID: 84964315276     PISSN: None     EISSN: 14712156     Source Type: Journal    
DOI: 10.1186/s12863-014-0136-1     Document Type: Article
Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.