| Q33901563 | ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cells. |
| Q24650370 | Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family |
| Q33855114 | Autosomal recessive nonsyndromic hearing loss |
| Q33639128 | Beginning of a molecular era in hearing and deafness |
| Q33200504 | Characterisation of DRASIC in the mouse inner ear. |
| Q34125294 | DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34. |
| Q28582690 | Expression of epithelial calcium transport system in rat cochlea and vestibular labyrinth. |
| Q28628858 | Isolation and characterization of a human thiamine pyrophosphokinase cDNA |
| Q35105506 | Novel autosomal recessive nonsyndromic hearing impairment locus DFNB90 maps to 7p22.1-p15.3. |
| Q55618045 | PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disorders. |
| Q36844240 | The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from Pakistan |
| Q24291227 | The human contactin-associated protein-like 2 gene (CNTNAP2) spans over 2 Mb of DNA at chromosome 7q35 |