Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7

American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

Volumn 163, Issue 3, 2013, Pages 178-184

  Vermeer, Alexa M C ^a   van Engelen, Klaartje ^a   Postma, Alex V ^a   Baars, Marieke J H ^a   Christiaans, Imke ^a   De Haij, Simone ^e   Klaassen, Sabine ^b,c   Mulder, Barbara J M ^a   Keavney, Bernard ^d  

^a ACADEMIC MEDICAL CENTER   (Netherlands)

^b CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^c MAX DELBRÜCK CENTER FOR MOLECULAR MEDICINE   (Germany)

^d UNIVERSITY OF MANCHESTER   (United Kingdom)

^e University of Manchester ^*

Author keywords

Cardiomyopathy; Ebstein anomaly; Genetics; Heart defects, congenital; Isolated noncompaction of the left ventricular myocardium; MYH7

Indexed keywords

ACTIN; ALPHA CARDIAC ACTIN 1; ALPHA TROPOMYOSIN; BINDING PROTEIN; CARDIAC MYOSIN BINDING PROTEIN C; LITHIUM; MYOSIN HEAVY CHAIN BETA; TRANSCRIPTION FACTOR NKX2.5; TROPONIN I; TROPONIN T; UNCLASSIFIED DRUG; CARDIAC MYOSIN; MYH7 PROTEIN, HUMAN; MYOSIN HEAVY CHAIN;

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHROMOSOME 1P; CHROMOSOME DELETION; CYANOSIS; DISEASE ASSOCIATION; DNA SEQUENCE; EBSTEIN ANOMALY; HEART ATRIUM SEPTUM DEFECT; HEART FAILURE; HEART MUSCLE; HUMAN; INHERITANCE; INTRAUTERINE INFECTION; LINKAGE ANALYSIS; MISSENSE MUTATION; PATENT FORAMEN OVALE; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SUDDEN CARDIAC DEATH; THROMBOEMBOLISM; TRANSTHORACIC ECHOCARDIOGRAPHY; VENTRICULAR NONCOMPACTION; COMPLICATION; DOMINANT GENE; GENETICS; HEART VENTRICLE; MUTATION;

CARDIAC MYOSINS; EBSTEIN ANOMALY; GENES, DOMINANT; HEART VENTRICLES; HUMANS; ISOLATED NONCOMPACTION OF THE VENTRICULAR MYOCARDIUM; MUTATION; MYOSIN HEAVY CHAINS; PHENOTYPE;

EID: 84880700979     PISSN: 15524868     EISSN: 15524876     Source Type: Journal    
DOI: 10.1002/ajmg.c.31365     Document Type: Article

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