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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.