The phenotype of DFNA13/COL11A2: Nonsyndromic autosomal dominant mid-frequency and high-frequency sensorineural hearing impairment.
SourceAmerican Journal of Otology, 21, (2000), pp. 181-187
Article / Letter to editor
Display more detailsDisplay less details
American Journal of Otology
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.