References
- BorckG.RainshteinL.Hellman-AharonyS.VolkA.E.FriedrichK.TaubE.et al. 2012. High frequency of autosomal-recessive DFNB59 hearing loss in an isolated Arab population in Israel. Clinical Genetics, 82: 271–276.
- ChaleshtoriM.H.SimpsonM.A.FarrokhiE.DolatiM.Hoghooghi RadL.Amani GeshniganiS.et al. 2007. Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families. Clinical Genetics, 72: 261–263.
- CollinR.W.KalayE.OostrikJ.CaylanR.WollnikB.ArslanS.et al. 2007. Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment. Human Mutation, 28: 718–723.
- DelmaghaniS.del CastilloF.J.MichelV.LeiboviciM.AghaieA.RonU.et al. 2006. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nature Genetics, 38: 770–778.
- EbermannI.WalgerM.SchollH.P.CharbelI.P.LuekeC.NuernbergG.et al. 2007. Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction. Human Mutation, 28: 571–577.
- LinthicumF.H.JrFayadJ.N. 2009. Spiral ganglion cell loss is unrelated to segmental cochlear sensory system degeneration in humans. Otology and Neurotology, 30: 418–422.
- LiuW.BoströmM.KinneforsA.LinthicumF.H.JrRask-AndersenH. 2012. Expression of myelinbasic protein in the human auditory nerve – an immunohistochemical and comparative study. Auris, Nasus, Larynx, 39: 18–24.
- LiuW.BoströmM.KinneforsA.Rask-AndersenH. 2009a. Unique expression of connexins in the human cochlea. Hearing Research, 250: 55–62.
- LiuW.BoströmM.Rask-AndersenH. 2009b. Expression of peripherin in the pig spiral ganglion – aspects of nerve injury and regeneration. Acta Otolaryngologica, 129: 608–614.
- LiuW.KinneforsA.BoströmM.Rask-AndersenH. 2010. Expression of peripherin in human cochlea. Cell and Tissue Research, 342: 345–351.
- MujtabaG.BukhariI.FatimaA.NazS. 2012. A p.C343S missense mutation in PJVK causes progressive hearing loss. Gene, 504: 98–101.
- SchwanderM.SczanieckaA.GrilletN.BaileyJ.S.AvenariusM.NajmabadiH.et al. 2007. A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. Journal of Neuroscience, 28: 2163–2175.
- SiningerY. 2002. Identification of auditory neuropathy in infants and children. Seminars in Hearing, 23: 193–200.