Genetic information register for families with an inherited cardiac condition (Oxfordshire REC C Ref: 09/H0606/108)
Currently recruiting patients:
- referred or eligible for clinical genetic testing (mutation screen or familial test)
- for an inherited cardiomyopathy or channelopathy (including HCM, DCM, Long QT, Brugada syndrome, ARVC, metabolic/syndromic cardiomyopathy)
- participants may or may not be clinically affected
- no age limit
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.