Jeroen J. Smits
- A RIPOR2 in-frame deletion is a frequent and highly penetrant cause of adult-onset hearing loss
2020/07/06 by Suzanne E de Bruijn, Suzanne E. de Bruijn, Jeroen J. Smits +23 · 11 citations
Biochemistry, Genetics and Molecular Biology · Medicine · Neuroscience · #Audiology #Biology #Congenital hearing loss #Exome #Exome sequencing #Gene #Genetic heterogeneity #Genetics #Genomics and Rare Diseases #Hearing loss #Hearing, Cochlea, Tinnitus, Genetics #Medicine #Phenotype #Sensorineural hearing loss #Vestibular and auditory disorders