Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic tetralogy of fallot and double outlet right ventricle in a Chinese Han population

Molecular Biology Reports

Volumn 41, Issue 4, 2014, Pages 2671-2677

  Huang, Xiaomin ^a   Niu, Wenquan ^a   Zhang, Zhen ^a   Zhou, Chunxia ^a   Xu, Zhiwei ^a   Liu, Jinfen ^a   Su, Zhaokang ^a   Ding, Wenxiang ^a   Zhang, Haibo ^a  

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

Author keywords

Conotruncal defects (CTDs); Double outlet right ventricle (DORV); Tetralogy of Fallot (TOF); ZFPM2 FOG2

Indexed keywords

AMINO ACID SUBSTITUTION; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; EXON; FALLOT TETRALOGY; FEMALE; GENE; GENE MUTATION; GENETIC LINKAGE; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HEART RIGHT VENTRICLE DOUBLE OUTLET; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; ZINC FINGER PROTEIN FOG FAMILY MEMBER 2 GENE; ALLELE; AMINO ACID SEQUENCE; CASE CONTROL STUDY; GENE ORDER; GENETICS; GENOTYPE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; SINGLE NUCLEOTIDE POLYMORPHISM;

DNA BINDING PROTEIN; TRANSCRIPTION FACTOR; ZFPM2 PROTEIN, HUMAN;

ALLELES; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; DOUBLE OUTLET RIGHT VENTRICLE; EXONS; FEMALE; GENE ORDER; GENETIC LINKAGE; GENETIC VARIATION; GENOTYPE; HUMANS; INFANT; MALE; MOLECULAR SEQUENCE DATA; POLYMORPHISM, SINGLE NUCLEOTIDE; TETRALOGY OF FALLOT; TRANSCRIPTION FACTORS;

EID: 84897492341     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-014-3126-5     Document Type: Article

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