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Mahmood, U., Bukhari, S.A., Ali, M., Ahmed, Z.M., Riazuddin S., 2021. Identification of hearing loss-associated variants of PTPRQ, MYO15A, and SERPINB6 in pakistani families. Biomed. Res. Int. 2021, 5584788
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Scarff, K.L., Ung, K.S., Nandurkar, H., Crack, P.J., Bird, C.H. Bird, P.I., 2004. Targeted disruption of SPI3/Serpinb6 does not result in developmental or growth defects, leukocyte dysfunction, or susceptibility to stroke. Mol. Cell Biol. 24, 4075-4082
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Silverman, G.A., Whisstock, J.C., Askew, D.J., Pak, S.C., Luke, C.J. Cataltepe, S., Irving, J.A., Bird, P.I., 2004. Human clade B serpins (ov-serpins) belong to a cohort of evolutionarily dispersed intracellular proteinase inhibitor clades that protect cells from promiscuous proteolysis. Cell. Mol. Life Sci. 61: 301-325
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Sirmaci, A., Erbek, S., Price, J., Huang, M.Q., Duman, D. Cengiz, F.B., Bademci, G., Tokgoz-Yilmaz, S., Hismi, B., Ozdag, H., 2010. A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss. Am. J. Human Genet. 86, 797-804
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Tan, J., Kaiserman, D., O'leary, S.J., Bird, P.I., 2021a. Increased susceptibility to acoustic trauma in a mouse model of non-syndromic sensorineural deafness, DFNB91. Eur. J. Neurosci 53, 1638-1651
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Tan, J., Kaiserman D., O'leary, S.J., Bird, P.I., 2021b. Mice heterozygous for the Serpinb6a null mutation show deficits in central auditory function after acoustic trauma. Neuroreport 32, 1287-1292
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Tan, J., Prakash, M.D., Kaiserman, D., Bird, P.I., 2013. Absence of SERPINB6A causes sensorineural hearing loss with multiple histopathologies in the mouse inner ear. Am. J. Pathol. 183, 49-59
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