A new gene is linked to primary ciliary dyskinesia (PCD), a rare disease that affects the airways. Using whole exome sequencing and bioinformatic analysis, researchers from the Genetic Disorders of Mucociliary Clearance Consortium (GDMCC) identified a variant in the CFAP57 gene that causes PCD, as published in the journal PLOS Genetics.

Presenting: #mydystonia&I Webinar Series

Dystonia: The Mysterious Disorder Impacting 50,000 Canadians

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On behalf of the DMRF Canada Board of Directors, and grant sponsor Jackson Mooney, we are pleased to announce the recipients of the 2020 Jackson Mooney Patient Grant for Dystonia.