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Molecular genetic studies of individuals and families at risk of inherited cardiac disease (REC Approval Number 09/H0605/3)

Many people clinically affected with cardiomyopathy or cardiac arrhythmia do not have a detectable mutation in the genes currently tested, possibly because the causal mutation may be in a gene not yet identified. This study aims to investigate additional biological candidate genes, and to identify new candidate genes by family linkage studies.

Individuals/families with unusual clinical manifestations or patterns of inheritance, or classical disease but in whom no mutation can be detected, are the focus of this research study.

If you are a researcher and would like to know more about this study, or if you have similar research interests, please contact the research team.