“We couldn’t be more excited to be working with a true innovator in Perlara. Their dedication and devotion to work with families to find cures was evident on our first call. Our daughter, Maggie, has an amazing spirit and is working hard – be it in physical therapy or in her school – on a daily basis. As parents we feel we owe it to her to do whatever we can to find a treatment and we are overjoyed to be working with Perlara on Maggie’s journey.”
— Holly and Dan Carmichael, Founders of Maggie’s PMM2-CDG Cure
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PerlQuest updates from our Blog
Perlara PBC and Maggie’s Cure have started a PerlQuest for a glycosylation disorder called PMM-2 deficiency disease - one of the most common congenital disorders of...
A goal of Stage 1 of our PMM2-CDG PerlQuest with Maggie’s Cure is to identify yeast models that are suitable for use in screens for small molecules that rescue PMM2...