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A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy

Varnava, A; Baboonian, C; Davison, F; de Cruz, L; Elliott, PM; Davies, MJ; McKenna, WJ (1999) A new mutation of the cardiac troponin T gene causing familial hypertrophic cardiomyopathy without left ventricular hypertrophy. HEART, 82 (5). 621 - 624 (4). ISSN 1355-6037
SGUL Authors: Baboonian, Christina

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Item Type: Article
Additional Information: PubMed ID: 10525521
Keywords: Adult, Cardiomyopathy, Hypertrophic, DNA Mutational Analysis, Death, Sudden, Cardiac, Female, Genetic Testing, Humans, Male, Middle Aged, Mutation, Missense, Pedigree, Polymerase Chain Reaction, Sarcomeres, Troponin T, Science & Technology, Life Sciences & Biomedicine, Cardiac & Cardiovascular Systems, Cardiovascular System & Cardiology, hypertrophic cardiomyopathy, troponin T, MYOSIN HEAVY-CHAIN, PROTEIN-C GENE, BETA-MYOSIN, MYOCARDIAL DISARRAY, SKELETAL-MUSCLE, EXPRESSION, hypertrophic cardiomyopathy, troponin T
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title: HEART
ISSN: 1355-6037
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Dates:
DateEvent
1 November 1999Published
Web of Science ID: WOS:000083536600022
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URI: https://openaccess.sgul.ac.uk/id/eprint/27

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