Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies

Cardiology in the Young

Volumn 22, Issue 2, 2012, Pages 194-201

  Ma, Lijiang ^a   Tierney, Elif Seda Selamet ^b   Lee, Teresa ^a   Lanzano, Patricia ^a   Chung, Wendy K ^a  

^a Medical Center ^*  (United States)

^b STANFORD UNIVERSITY   (United States)

Author keywords

CFC1; congenital cardiac defect; Left right asymmetry; LEFTYA

Indexed keywords

ACTIVIN A RECEPTOR TYPE 2B; ACTIVIN RECEPTOR; CRYPTIC PROTEIN; EPIDERMAL GROWTH FACTOR; LEFT RIGHT DETERMINATION FACTOR; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN; ZINC FINGER PROTEIN OF THE CEREBELLUM 3;

ACTIVIN A RECEPTOR TYPE 2B GENE; AFRICAN AMERICAN; ARTICLE; ASIAN; CAUCASIAN; CHILD; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CRYPTIC GENE; FEMALE; FETUS; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENETIC VARIABILITY; GREAT VESSELS TRANSPOSITION; HEART ATRIUM SEPTUM DEFECT; HEART DEVELOPMENT; HEART VENTRICLE SEPTUM DEFECT; HETEROTAXY SYNDROME; HISPANIC; HUMAN; LEFT RIGHT DETERMINATION FACTOR 2 GENE; LUNG VEIN DRAINAGE ANOMALY; MALE; MISSENSE MUTATION; PATHOGENESIS; POLYMERASE CHAIN REACTION; PREDICTION; PROTEIN FUNCTION; PULMONARY VEIN MALFORMATION; SEQUENCE ANALYSIS; ZINC FINGER PROTEIN OF THE CEREBELLUM 3 GENE;

ACTIVIN RECEPTORS, TYPE II; CARDIOVASCULAR ABNORMALITIES; CASE-CONTROL STUDIES; FEMALE; FETUS; GENOTYPE; HETEROTAXY SYNDROME; HOMEODOMAIN PROTEINS; HUMANS; INTERCELLULAR SIGNALING PEPTIDES AND PROTEINS; LEFT-RIGHT DETERMINATION FACTORS; MALE; MUTATION; NEW YORK CITY; PREGNANCY; SEQUENCE ANALYSIS; TRANSCRIPTION FACTORS;

EID: 84863243848     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951111001181     Document Type: Article

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