| 1 | CLDN9, DFNB116 |
| Variants of human CLDN9 cause mild to profound hearing loss. | |
| Ramzan M, Philippe C, Belyantseva IA, Nakano Y, Fenollar-Ferrer C, Tona R, Yousaf R, Basheer R, Imtiaz A, Faridi R, Munir Z, Idrees H, Salman M, Nambot S, Vitobello A, Kartti S, Zarrik O, Witmer PD, Sobreria N, Ibrahimi A, Banfi B, Moutton S, Friedman TB, Naz S. | |
| Hum Mutat. Oct;42(10):1321-1335. doi: 10.1002/humu.24260. Epub 2021 Aug 1. 2021 | |
| 2 | CLDN9, DFNB116 |
| A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss | |
| Sineni CJ, Yildirim-Baylan M, Guo S, Camarena V, Wang G, Tokgoz-Yilmaz S, Duman D, Bademci G, Tekin M. | |
| Hum Genet. Oct;138(10):1071-1075. doi: 10.1007/s00439-019-02037-1. Epub 2019 Jun 7. 2019 | |