Joining the Registry
If you or someone in your family has LMNA-related cardiomyopathy or may have any condition originating from an LMNA variant, consider joining our registry to help us create a more personalized care plan and investigate the associations between the LMNA gene and clinical presentations.
Eligibility Criteria:
- Disease-associated variant in the gene LMNA
- Willingness to share medical records to confirm the diagnosis and genetic variant (this will be kept strictly confidential)
- Willingness to provide a DNA sample (such as a saliva sample)
*Note: please turn off any pop-up blockers to access the enrollment form!
Consent Forms
If you are interested in joining the registry, feel free to take a look at the corresponding consent forms.
Contact Us
We understand that you may have many questions about LMNA, which can be a difficult set of processes to search through. We have listed some beginning resources but if you find you still have questions, feel free to reach out to our lead Research Scientist Gabrielle Monaco!
