| 1 | DFNB89 |
| DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2. | |
| Basit S, Lee K, Habib R, Chen L, Umm-E-Kalsoom, Santos-Cortez RL, Azeem Z, Andrade P, Ansar M, Ahmad W, Leal SM. | |
| Hum Genet 129(4):379-85. Epub 2010 Dec 22. 2011 | |