NALCN – UNC80 Research advances CLIFAHDD and IHPRF Syndrome

Fundación Libellas. September 2020. Newsletter. https:fundacionlibellas.org Our understanding of the NALCN protein complex responsible for the CLIFAHDD and IHPRF1&2 syndromes has reached new milestones over the last months. Two recent…

Continue Reading NALCN – UNC80 Research advances CLIFAHDD and IHPRF Syndrome

NALCN – UNC80 Research advances CLIFAHDD and IHPRF Syndrome

Fundación Libellas. September 2020. Newsletter. https:fundacionlibellas.org Our understanding of the NALCN protein complex responsible for the CLIFAHDD and IHPRF1&2 syndromes has reached new milestones over the last months. Two recent…

Continue Reading NALCN – UNC80 Research advances CLIFAHDD and IHPRF Syndrome

JOIN IN ON THE ACTION! RARE DISEASE DAY

February 28, 2021 Rare disease day takes place on the last day of February each year. The main objective of Rare Disease Day is to raise awareness among the general public and decision-makers about rare diseases…

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Fundación Libellas is a Proud REN and EURORDIS member!

Rare diseases and rare epilepsies collaborating! As part of REN, we look forward to learning from and sharing our knowledge with a whole patient engagement community. https://www.rareepilepsynetwork.org/ By joining forces,…

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