TY - JOUR AU - Morton, N. E. PY - 1991 DA - 1991// TI - Genetic epidemiology of hearing impairment JO - Ann N Y Acad Sci VL - 630 UR - https://doi.org/10.1111/j.1749-6632.1991.tb19572.x DO - 10.1111/j.1749-6632.1991.tb19572.x ID - Morton1991 ER - TY - JOUR AU - Morton, C. C. AU - Nance, W. E. PY - 2006 DA - 2006// TI - Newborn hearing screening--a silent revolution JO - N Engl J Med VL - 354 UR - https://doi.org/10.1056/NEJMra050700 DO - 10.1056/NEJMra050700 ID - Morton2006 ER - TY - JOUR AU - Morton, C. C. PY - 2002 DA - 2002// TI - Genetics, genomics and gene discovery in the auditory system JO - Hum Mol Genet VL - 11 UR - https://doi.org/10.1093/hmg/11.10.1229 DO - 10.1093/hmg/11.10.1229 ID - Morton2002 ER - TY - JOUR AU - Smith, R. J. AU - Bale, J. F. AU - White, K. R. PY - 2005 DA - 2005// TI - Sensorineural hearing loss in children JO - Lancet VL - 365 UR - https://doi.org/10.1016/S0140-6736(05)71047-3 DO - 10.1016/S0140-6736(05)71047-3 ID - Smith2005 ER - TY - JOUR AU - Parker, M. A. PY - 2011 DA - 2011// TI - Biotechnology in the treatment of sensorineural hearing loss: foundations and future of hair cell regeneration JO - J Speech Lang Hear Res VL - 54 UR - https://doi.org/10.1044/1092-4388(2011/10-0149) DO - 10.1044/1092-4388(2011/10-0149) ID - Parker2011 ER - TY - JOUR AU - Nakagawa, T. PY - 2014 DA - 2014// TI - Strategies for developing novel therapeutics for sensorineural hearing loss JO - Front Pharmacol VL - 5 UR - https://doi.org/10.3389/fphar.2014.00206 DO - 10.3389/fphar.2014.00206 ID - Nakagawa2014 ER - TY - JOUR PY - 2002 DA - 2002// TI - Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement JO - Genet Med VL - 4 UR - https://doi.org/10.1097/00125817-200205000-00011 DO - 10.1097/00125817-200205000-00011 ID - ref7 ER - TY - JOUR AU - Mahboubi, H. AU - Dwabe, S. AU - Fradkin, M. AU - Kimonis, V. AU - Djalilian, H. R. PY - 2012 DA - 2012// TI - Genetics of hearing loss: where are we standing now? JO - Eur Arch Otorhinolaryngol VL - 269 UR - https://doi.org/10.1007/s00405-011-1910-6 DO - 10.1007/s00405-011-1910-6 ID - Mahboubi2012 ER - TY - JOUR AU - Thirlwall, A. S. AU - Brown, D. J. AU - McMillan, P. M. AU - Barker, S. E. AU - Lesperance, M. M. PY - 2003 DA - 2003// TI - Phenotypic characterization of hereditary hearing impairment linked to DFNA25 JO - Arch Otolaryngol Head Neck Surg VL - 129 UR - https://doi.org/10.1001/archotol.129.8.830 DO - 10.1001/archotol.129.8.830 ID - Thirlwall2003 ER - TY - JOUR AU - Park, M. K. AU - Sagong, B. AU - Lee, J. D. AU - Bae, S. H. AU - Lee, B. AU - Choi, K. S. PY - 2014 DA - 2014// TI - A1555G homoplasmic mutation from A1555G heteroplasmic mother with Pendred syndrome JO - Int J Pediatr Otorhinolaryngol VL - 78 UR - https://doi.org/10.1016/j.ijporl.2014.08.009 DO - 10.1016/j.ijporl.2014.08.009 ID - Park2014 ER - TY - JOUR AU - Greene, C. C. AU - McMillan, P. M. AU - Barker, S. E. AU - Kurnool, P. AU - Lomax, M. I. AU - Burmeister, M. PY - 2001 DA - 2001// TI - DFNA25, a novel locus for dominant nonsyndromic hereditary hearing impairment, maps to 12q21-24 JO - Am J Hum Genet VL - 68 UR - https://doi.org/10.1086/316925 DO - 10.1086/316925 ID - Greene2001 ER - TY - JOUR AU - Camp, G. AU - Willems, P. J. AU - Smith, R. J. PY - 1997 DA - 1997// TI - Nonsyndromic hearing impairment: unparalleled heterogeneity JO - Am J Hum Genet VL - 60 ID - Camp1997 ER - TY - JOUR AU - Ruel, J. AU - Emery, S. AU - Nouvian, R. AU - Bersot, T. AU - Amilhon, B. AU - Rybroek, J. M. PY - 2008 DA - 2008// TI - Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice JO - Am J Hum Genet VL - 83 UR - https://doi.org/10.1016/j.ajhg.2008.07.008 DO - 10.1016/j.ajhg.2008.07.008 ID - Ruel2008 ER - TY - JOUR AU - Fremeau, R. T. AU - Burman, J. AU - Qureshi, T. AU - Tran, C. H. AU - Proctor, J. AU - Johnson, J. PY - 2002 DA - 2002// TI - The identification of vesicular glutamate transporter 3 suggests novel modes of signaling by glutamate JO - Proc Natl Acad Sci U S A VL - 99 UR - https://doi.org/10.1073/pnas.222546799 DO - 10.1073/pnas.222546799 ID - Fremeau2002 ER - TY - JOUR AU - Almqvist, J. AU - Huang, Y. AU - Laaksonen, A. AU - Wang, D. N. AU - Hovmoller, S. PY - 2007 DA - 2007// TI - Docking and homology modeling explain inhibition of the human vesicular glutamate transporters JO - Protein Sci VL - 16 UR - https://doi.org/10.1110/ps.072944707 DO - 10.1110/ps.072944707 ID - Almqvist2007 ER - TY - JOUR AU - Pao, S. S. AU - Paulsen, I. T. AU - Saier, M. H. PY - 1998 DA - 1998// TI - Major facilitator superfamily JO - Microbiol Mol Biol Rev VL - 62 ID - Pao1998 ER - TY - JOUR AU - Seal, R. P. AU - Akil, O. AU - Yi, E. AU - Weber, C. M. AU - Grant, L. AU - Yoo, J. PY - 2008 DA - 2008// TI - Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3 JO - Neuron VL - 57 UR - https://doi.org/10.1016/j.neuron.2007.11.032 DO - 10.1016/j.neuron.2007.11.032 ID - Seal2008 ER - TY - JOUR AU - Dror, A. A. AU - Avraham, K. B. PY - 2010 DA - 2010// TI - Hearing impairment: a panoply of genes and functions JO - Neuron VL - 68 UR - https://doi.org/10.1016/j.neuron.2010.10.011 DO - 10.1016/j.neuron.2010.10.011 ID - Dror2010 ER - TY - JOUR AU - Stelma, F. AU - Bhutta, M. F. PY - 2014 DA - 2014// TI - Non-syndromic hereditary sensorineural hearing loss: review of the genes involved JO - J Laryngol Otol VL - 128 UR - https://doi.org/10.1017/S0022215113003265 DO - 10.1017/S0022215113003265 ID - Stelma2014 ER - TY - JOUR AU - Takamori, S. AU - Malherbe, P. AU - Broger, C. AU - Jahn, R. PY - 2002 DA - 2002// TI - Molecular cloning and functional characterization of human vesicular glutamate transporter 3 JO - EMBO Rep VL - 3 UR - https://doi.org/10.1093/embo-reports/kvf159 DO - 10.1093/embo-reports/kvf159 ID - Takamori2002 ER - TY - JOUR AU - Kim, M. A. AU - Kim, Y. R. AU - Sagong, B. AU - Cho, H. J. AU - Bae, J. W. AU - Kim, J. PY - 2014 DA - 2014// TI - Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss JO - PLoS One VL - 9 UR - https://doi.org/10.1371/journal.pone.0095646 DO - 10.1371/journal.pone.0095646 ID - Kim2014 ER - TY - JOUR AU - Kim, Y. R. AU - Kim, M. A. AU - Sagong, B. AU - Bae, S. H. AU - Lee, H. J. AU - Kim, H. J. PY - 2015 DA - 2015// TI - Evaluation of the contribution of the EYA4 and GRHL2 genes in Korean patients with autosomal dominant non-syndromic hearing loss JO - PLoS One VL - 10 UR - https://doi.org/10.1371/journal.pone.0119443 DO - 10.1371/journal.pone.0119443 ID - Kim2015 ER - TY - JOUR AU - Lee, K. Y. AU - Choi, S. Y. AU - Bae, J. W. AU - Kim, S. AU - Chung, K. W. AU - Drayna, D. PY - 2008 DA - 2008// TI - Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients JO - Int J Pediatr Otorhinolaryngol VL - 72 UR - https://doi.org/10.1016/j.ijporl.2008.05.007 DO - 10.1016/j.ijporl.2008.05.007 ID - Lee2008 ER -