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
Full text not available from this repository.
Item Type: |
Article
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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 |
Related URLs: |
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Dates: |
Date | Event |
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1 November 1999 | Published |
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Web of Science ID: |
WOS:000083536600022 |
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URI: |
https://openaccess.sgul.ac.uk/id/eprint/27 |
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