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DNA connections

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

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

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

The PLN Foundation in The Netherlands is looking for a scientifically skilled person for 16 hours a week. Read more…
Read moreSponsor the cycle tour of Daan!

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

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