| 1 | DFNB22, OTOA
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| Targeted next-generation sequencing and parental genotyping in sporadic Chinese Han deaf patients.
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| He L, Pang X, Liu H, Chai Y, Wu H, Yang T.
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| Clin Genet 93(4):899-904. doi: 10.1111/cge.13182. Epub 2018 Feb 20.
2018
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| 2 | OTOA
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| Increased Spontaneous Otoacoustic Emissions in Mice with a Detached Tectorial Membrane.
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| Cheatham MA, Ahmad A, Zhou Y, Goodyear RJ, Dallos P, Richardson GP.
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| J Assoc Res Otolaryngol 17(2):81-8. doi: 10.1007/s10162-015-0551-7. Epub 2015 Dec 21.
2016
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| 3 | OTOA
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| Effect of the attachment of the tectorial membrane on cochlear micromechanics and two-tone suppression.
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| Meaud J, Grosh K.
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| Biophys J 106(6):1398-405. doi: 10.1016/j.bpj.2014.01.034.
2014
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| 4 | DFNB22, OTOA
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| Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.
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| Lee K, Chiu I, Santos-Cortez RL, Basit S, Khan S, Azeem Z, Andrade PB, Kim SS, Ahmad W, Leal SM.
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| Clin Genet 84(3):294-6. doi: 10.1111/cge.12047. Epub 2012 Nov 23. No abstract available.
2013
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| 5 | DFNB22, OTOA
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| A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation.
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| Lukashkin AN, Legan PK, Weddell TD, Lukashkina VA, Goodyear RJ, Welstead LJ, Petit C, Russell IJ, Richardson GP.
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| Proc Natl Acad Sci U S A 109(47):19351-6. doi: 10.1073/pnas.1210159109. Epub 2012 Nov 5.
2012
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| 6 | DFNB22, OTOA
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| Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.
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| Zwaenepoel I, Mustapha M, Leibovici M, Verpy E, Goodyear R, Liu XZ, Nouaille S, Nance WE, Kanaan M, Avraham KB, Tekaia F, Loiselet J, Lathrop M, Richardson G, Petit C.
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| Proc Natl Acad Sci U S A 99(9):6240-5. 2002
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