De novo variants are a common cause of genetic hearing loss
Miles J. Klimara, Carla Nishimura, Donghong Wang, Diana L. Kolbe, Amanda M. Schaefer, William D. Walls, Kathy L. Frees, Richard J. Smith, Héla Azaiez
Topics & Concepts
GeneticsBiologyProbandMassive parallel sequencingHearing lossGenetic heterogeneityGenetic analysisGenePhenotypeMutationDNA sequencingMedicineAudiologyHearing, Cochlea, Tinnitus, GeneticsGenomics and Rare DiseasesGenetic Neurodegenerative Diseases