Identification of Genetic Variants in CFAP221 as a Cause of Primary Ciliary Dyskinesia

Don and Wu-Lin’s paper with collaborators at UNC – describing work they did to use PSAP to find a novel cause of PCD – is now available online in the Journal of Human Genetics. Congratulations! Abstract Primary ciliary dyskinesia (PCD) is a rare disorder that affects the biogenesis or function of motile cilia resulting in […]