PLN Heart Foundation
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Menu
  • What is PLN
    • The Gene and Symptoms
    • Diagnosis and Treatment
    • Facts and Figures
    • Frequently Asked Questions (FAQ)
    • Heredity
  • Patients and Relatives
    • Family Members
    • Patients contact
    • Experiences and stories
    • Employers
    • Read and watch
    • Thematic information
  • PLN Foundation
    • PLN Foundation
    • Team
    • Collaborations
    • About Us
    • Contact
    • Complaints procedure
    • Polls
  • Research
    • Research
    • Network
  • News and Events
    • News
    • PLN Elfstedentocht
    • Events
Help me

PLN Heart Disease Foundation. For patients, by patients.

Founded by volunteers and people suffering from PLN heart muscle disease, family members and their loved ones, our foundation seeks to inform people with the PLN gene about the latest developments and studies on PLN.

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What can you do?

Help us overcome the genetic heart muscle disease PLN

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