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

Full text not available from this repository.

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 and Allied Health Education (IMBE) Academic Structure > Institute of Medical, Biomedical and Allied Health Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title:	J Med Genet
PubMed ID:	10978365
Web of Science ID:	10978365
	Download EPMC Full text (PDF)
	Download EPMC Full text (HTML)
	Go to PubMed abstract
URI:	https://openaccess.sgul.ac.uk/id/eprint/171

Actions (login required)

Edit Item