Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot

International Journal of Molecular Medicine

Volumn 31, Issue 1, 2013, Pages 51-58

  Huang, Ri Tai ^a   Xue, Song ^a   Xu, Ying Jia ^b   Yang, Yi Qing ^b  

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

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

Author keywords

Congenital heart disease; GATA6; Genetics; Reporter gene analysis; Tetralogy of Fallot; Transcription factor

Indexed keywords

LUCIFERASE; TRANSCRIPTION FACTOR GATA 6;

ARTICLE; BLOOD SAMPLING; CHILD; FALLOT TETRALOGY; FEMALE; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC TRANSCRIPTION; GENOTYPE; HEART VALVE REPLACEMENT; HETEROZYGOTE; HUMAN; HUMAN CELL; HUMAN TISSUE; INFANT; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PRESCHOOL CHILD; PRIORITY JOURNAL; REPORTER GENE; RHEUMATIC HEART DISEASE; SCHOOL CHILD; SEQUENCE ANALYSIS; SOMATIC MUTATION; TRANSCRIPTION INITIATION; WILD TYPE;

AMINO ACID SEQUENCE; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GATA6 TRANSCRIPTION FACTOR; GENES, REPORTER; GENETIC PREDISPOSITION TO DISEASE; GENOME, HUMAN; GENOTYPE; HEART; HETEROZYGOTE; HUMANS; INFANT; MALE; MOLECULAR SEQUENCE DATA; MUTATION; SEQUENCE ALIGNMENT; TETRALOGY OF FALLOT; TRANSCRIPTIONAL ACTIVATION;

EID: 84873174654     PISSN: 11073756     EISSN: 1791244X     Source Type: Journal    
DOI: 10.3892/ijmm.2012.1188     Document Type: Article

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