Thoracic aortic-aneurysm and dissection in association with significant mitral valve disease caused by mutations in TGFB2

International Journal of Cardiology

Volumn 165, Issue 3, 2013, Pages 584-587

  Renard, Marjolijn ^a   Callewaert, Bert ^a   Malfait, Fransiska ^a   Campens, Laurence ^a   Sharif, Saba ^b   Del Campo, Miguel ^c   Valenzuela, Irene ^c   McWilliam, Catherine ^d   Coucke, Paul ^a   De Paepe, Anne ^a   De Backer, Julie ^a  

^a GHENT UNIVERSITY HOSPITAL   (Belgium)

^b BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^c Institut Catala de Salut   (Spain)

^d Clinical Genetics Centre   (United Kingdom)

Author keywords

Genetics; Mitral valve disease; TGF beta; Thoracic aortic aneurysm

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA2;

ADULT; AGED; AORTA DISSECTION; AORTA ROOT; CATARACT; CLINICAL FEATURE; DISEASE ASSOCIATION; ECHOCARDIOGRAPHY; EXON; FEMALE; GENE AMPLIFICATION; GENE MUTATION; GENE SEQUENCE; GENETIC ASSOCIATION; HEART DILATATION; HETEROZYGOSITY; HUMAN; INTRON; LETTER; LOEYS DIETZ SYNDROME; MAJOR CLINICAL STUDY; MALE; MARFAN SYNDROME; MISSENSE MUTATION; MITRAL VALVE DISEASE; MITRAL VALVE PROLAPSE; MYOPIA; OSTEOARTHRITIS; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SEQUENCE ALIGNMENT; TGFB2 GENE; THORACIC AORTA ANEURYSM; THORACIC AORTA ANEURYSM AND DISSECTION; GENETIC HETEROGENEITY; GENETIC SCREENING; LOSS OF FUNCTION MUTATION; NONHUMAN; PATHOGENESIS;

EID: 84877021727     PISSN: 01675273     EISSN: 18741754     Source Type: Journal    
DOI: 10.1016/j.ijcard.2012.09.029     Document Type: Article

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