GATA5 loss-of-function mutations underlie tetralogy of fallot

International Journal of Medical Sciences

Volumn 10, Issue 1, 2012, Pages 34-42

  Wei, Dong ^a   Bao, Han ^a   Liu, Xing Yuan ^a   Zhou, Ning ^a   Wang, Qian ^b   Li, Ruo Gu ^b   Xu, Ying Jia ^b   Yang, Yi Qing ^b  

^a TONGJI UNIVERSITY SCHOOL OF MEDICINE   (China)

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

Author keywords

Congenital heart disease; GATA5; Genetics; Tetralogy of fallot; Transcription factor

Indexed keywords

AMINO ACID; LUCIFERASE; TRANSCRIPTION FACTOR GATA 5;

ADULT; ALLELE; AMINO ACID SEQUENCE; ARTICLE; CHILD; CONTROLLED STUDY; ENZYME ASSAY; FALLOT TETRALOGY; FEMALE; GENE FUNCTION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC CONSERVATION; GENETIC VARIABILITY; HETEROZYGOTE; HUMAN; LOSS OF FUNCTION MUTATION; MAJOR CLINICAL STUDY; MALE; MOLECULAR EVOLUTION; MOLECULAR PATHOLOGY; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PEDIGREE ANALYSIS; PRESCHOOL CHILD; SEQUENCE ALIGNMENT; SITE DIRECTED MUTAGENESIS; TRANSCRIPTION FACTOR GATA 5 GENE; WILD TYPE;

CONGENITAL HEART DISEASE; GATA5.; GENETICS; TETRALOGY OF FALLOT; TRANSCRIPTION FACTOR;

ADOLESCENT; ADULT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; FEMALE; GATA5 TRANSCRIPTION FACTOR; HETEROZYGOTE; HUMANS; INFANT; MALE; MUTATION; PEDIGREE; POLYMORPHISM, GENETIC; SEQUENCE ALIGNMENT; TETRALOGY OF FALLOT;

EID: 84871353547     PISSN: 14491907     EISSN: None     Source Type: Journal    
DOI: 10.7150/ijms.5270     Document Type: Article

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