Some of these research projects include PLN p.Arg14del mutation carriers and their medical information. Examples are studies into the large variability in symptoms and signs of the disease. Fundamental studies to understand how the PLN mutation leads to disease and how the disease could be treated are also initiated.
Register now as PLN carrier!
If you are a PLN carrier living outside the Netherlands, please do not hesitate to fill out this form and indicate:
whether you want to be on the mailing list of our PLN Genetic Heart Disease Foundation;
whether we can share your information details with the PHORECAST researchers;
Your completion of the following registry form is important for both our Foundation and researchers, and all PLN carriers we would like to identify at an early stage and to provide them with the right medical treatment method.
Many thanks for your understanding and cooperation! Please feel free to contact us if questions appear.