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Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy.

D'Cruz, LG; Baboonian, C; Phillimore, HE; Taylor, R; Elliott, PM; Varnava, A; Davison, F; McKenna, WJ; Carter, ND (2000) Cytosine methylation confers instability on the cardiac troponin T gene in hypertrophic cardiomyopathy. J Med Genet, 37 (9). E18 - ?.
SGUL Authors: Baboonian, Christina

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Item Type: Article
Additional Information: PMCID: PMC1734704
Keywords: Amino Acid Sequence, Amino Acid Substitution, Base Sequence, Cardiomyopathy, Hypertrophic, Cytosine, DNA, DNA Methylation, DNA Mutational Analysis, Female, Humans, Molecular Sequence Data, Mutation, Myocardium, Point Mutation, Sequence Homology, Amino Acid, 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: J Med Genet
Dates:
DateEvent
September 2000Published
PubMed ID: 10978365
Web of Science ID: 10978365
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URI: http://openaccess.sgul.ac.uk/id/eprint/171

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