Sort   by:  
 Page size 
UnknownDe novo variants are a common cause of genetic hearing loss.
Not available
S-EPMC9729384 | biostudies-literature
UnknownSingle-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4<sup>-/-</sup> mouse.
Not available
S-EPMC10268361 | biostudies-literature
UnknownAssessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.
Not available
S-EPMC10182131 | biostudies-literature
UnknownThe natural history of OTOF-related auditory neuropathy spectrum disorders: a multicenter study.
Not available
S-EPMC9093589 | biostudies-literature
UnknownA synonymous variant in MYO15A enriched in the Ashkenazi Jewish population causes autosomal recessive hearing loss due to abnormal splicing.
Not available
S-EPMC8187401 | biostudies-literature
UnknownSafety of the PCSK9 inhibitor alirocumab: insights from 47 296 patient-years of observation.
Not available
S-EPMC11249957 | biostudies-literature
Sort   by:  
 Page size