| 1 | COCH, DFNA9, DFNB110 |
| Audiovestibular Phenotypes and Advanced Magnetic Resonance Imaging Features of Cochlin Gene Mutation Carriers. | |
| Conte G, Lo Russo F, Caschera L, Zanetti D, Castorina P, Sina C, Triulzi F, Di Berardino F. | |
| Audiol Neurootol. 24(4):166-173. doi: 10.1159/000501292. Epub 2019 Aug 7 2019 | |
| 2 | COCH, DFNB110 |
| Bi-allelic inactivating variants in the COCH gene cause autosomal recessive prelingual hearing impairment | |
| JanssensdeVarebeke SPF, Van Camp G, Peeters N, Elinck E, Widdershoven J, Cox T, Deben K, Ketelslagers K, Crins T, Wuyts W. | |
| Eur J Hum Genet. Apr;26(4):587-591. doi: 10.1038/s41431-017-0066-2. Epub 2018 Feb 15. 2018 | |