Two novel mutations of the IRX4 gene in patients with congenital heart disease

Human Genetics

Volumn 130, Issue 5, 2011, Pages 657-662

  Cheng, Zhi ^a,c   Wang, Jing ^a,c   Su, Dongmei ^a   Pan, Hong ^a   Huang, Guoying ^d   Li, Xiaotian ^d   Li, Zhongzhi ^e   Shen, Adong ^e   Xie, Xiaodong ^f   Wang, Binbin ^a,c   Ma, Xu ^a,b,c  

^a NATIONAL RESEARCH INSTITUTE FOR FAMILY PLANNING   (China)

^b WORLD HEALTH ORGANIZATION   (Switzerland)

^c GRADUATE SCHOOL OF PEKING UNION MEDICAL COLLEGE   (China)

^d CHILDREN S HOSPITAL OF FUDAN UNIVERSITY   (China)

^e CAPITAL MEDICAL UNIVERSITY   (China)

^f LANZHOU UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA; PROTEIN; PROTEIN RXRA; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR IRX4; UNCLASSIFIED DRUG;

AORTA COARCTATION; ARTICLE; BIOINFORMATICS; CHILD; CHINESE; CONGENITAL HEART DISEASE; CONTROLLED STUDY; FALLOT TETRALOGY; GENE MUTATION; GENE SEQUENCE; HEART ATRIUM SEPTUM DEFECT; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART VENTRICLE SEPTUM DEFECT; HETEROZYGOTE; HUMAN; HUMAN CELL; INFANT; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; PATENT DUCTUS ARTERIOSUS; PHENOTYPE; PRIORITY JOURNAL; PULMONARY VALVE ATRESIA; PULMONARY VALVE STENOSIS; SCHOOL CHILD; SEQUENCE ALIGNMENT;

AMINO ACID SEQUENCE; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CHILD; COHORT STUDIES; HEART DEFECTS, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; INFANT; MALE; MOLECULAR SEQUENCE DATA; MUTATION; RETINOID X RECEPTORS;

MAMMALIA; MUS;

EID: 80054725699     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-011-0996-7     Document Type: Article

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