Holt-Oram syndrome: Novel TBX5 mutation and associated anomalous right coronary artery

Cardiology in the Young

Volumn 21, Issue 3, 2011, Pages 351-353

  Vianna, Caio B ^a   Miura, Nana ^a   Pereira, Alexandre C ^a   Jatene, Marcelo B ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Congenital cardiac disease; genetics; ischaemic cardiac disease; septal defects

Indexed keywords

POLITEF; TRANSCRIPTION FACTOR TBX5;

ADULT; AMINO ACID SUBSTITUTION; AORTA SINUS; ARTICLE; ARTIFICIAL HEART PACEMAKER; ATRIOVENTRICULAR BLOCK; BRADYCARDIA; CASE REPORT; CINEANGIOCARDIOGRAPHY; COMPUTER ASSISTED TOMOGRAPHY; CONTRAST ENHANCEMENT; CORONARY ARTERY ANOMALY; DISEASE ASSOCIATION; ELECTROCARDIOGRAPHY; GENE IDENTIFICATION; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HEART MURMUR; HEART SURGERY; HOLT ORAM SYNDROME; HUMAN; HYPOKINESIA; LUNG ARTERY PRESSURE; MALE; MULTIDETECTOR COMPUTED TOMOGRAPHY; PHYSICAL EXAMINATION; QRS COMPLEX; RIGHT CORONARY ARTERY;

ABNORMALITIES, MULTIPLE; ADULT; CORONARY VESSEL ANOMALIES; HEART DEFECTS, CONGENITAL; HEART SEPTAL DEFECTS, ATRIAL; HUMANS; LOWER EXTREMITY DEFORMITIES, CONGENITAL; MALE; MUTATION; T-BOX DOMAIN PROTEINS; UPPER EXTREMITY DEFORMITIES, CONGENITAL;

EID: 79955984878     PISSN: 10479511     EISSN: 14671107     Source Type: Journal    
DOI: 10.1017/S1047951111000072     Document Type: Article

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