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DNA connections

March 4, 2021

Hello, my name is Annette Klinkert: 59 years old, PLN carrier, transplanted and volunteer at the PLN Foundation. As all…

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International Rare Disease Day

February 28, 2021

Today it is International Rare Disease Day. PLN is a rare disease. There are only 1500 carriers known in the…

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Heredity

February 25, 2021

The PLN mutation is a hereditary disease and is therefore passed on from generation to generation. The mutation inherits an…

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Job opening

February 18, 2021

The PLN Foundation in The Netherlands is looking for a scientifically skilled person for 16 hours a week. Read more…

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Sponsor the cycle tour of Daan!

February 11, 2021

Daan Obdeijn from The Netherlands is organizing a sponsor campaign for the PLN Foundation: he will cycle an “alternative Elfstedentocht”!…

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Happy holidays!

December 23, 2020

Dear reader, If someone had asked me about 2020 last year, I could never have predicted a pandemic. Full of…

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Join the fight against
PLN Genetic Heart Disease

By sponsoring our PLN transatlantic research project, you will be investing in a unique opportunity to accelerate the development of a curative treatment for heart disease.

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PLN Foundation. Foundation of patients for patients.

PLN Foundation

Our Foundation has been established by volunteers or people suffering from PLN, family members and their loved ones, and tries to inform PLN gene carriers as much as possible about the latest developments and PLN studies.

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