Viljem Julijan Association for Children with Rare Diseases 

  • drustvo@viljem-julijan.si

Cure for Cockayne Syndrome – type B

Cure for Cockayne Syndrome – type B

admin_3p8fkrsy

admin_3p8fkrsy

About admin

This author has not yet filled in any details.
So far admin has created 7 blog entries.

Organisation: Viljem Julijan Association for Children with Rare Diseases, Cesta Leona Dobrotinška 2, 3230 Šentjur, Slovenia, EU

E-mail: drustvo@viljem-julijan.si

Thank you for your donation ❤

Donation options:

Account: IBAN SI56 0400 0027 7357 570
SWIFT/BIC code: KBMASI2X
Organisation: Viljem Julijan Association for Children with Rare Diseases, Cesta Leona Dobrotinška 2, 3230 Šentjur, Slovenia, EU

© Copyright 2023 | All Rights Reserved

Go to Top