Missense Mutation | Genetic Disorders of Mucociliary Clearance Consortium

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A Previously-Funded NIH Rare Diseases Clinical Research Network Consortium

A change in one DNA base pair that changes a codon into a codon corresponding to a different amino acid.

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The Genetic Disorders of Mucociliary Clearance Consortium (GDMCC) is a previously funded research group of the Rare Diseases Clinical Research Network (RDCRN), which is funded by the National Institutes of Health (NIH) and led by the National Center for Advancing Translational Sciences (NCATS) through its Division of Rare Diseases Research Innovation (DRDRI). GDMCC received funding under grant number U54HL096458 as a collaboration between NCATS and the National Heart, Lung, and Blood Institute (NHLBI). This website is hosted by the network’s Data Management and Coordinating Center at Cincinnati Children’s Hospital Medical Center, which is funded by NCATS and the National Institute of Neurological Disorders and Stroke (NINDS) under grant number TR002818. The content of this website is solely the responsibility of the GDMCC administrative coordinating center at the University of North Carolina at Chapel Hill and does not necessarily represent the official views of the NIH.