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Page 1
Temperature sensitive auditory neuropathy.
Zhang Q, Lan L, Shi W, Yu L, Xie LY, Xiong F, Zhao C, Li N, Yin Z, Zong L, Guan J, Wang D, Sun W, Wang Q. Zhang Q, et al. Among authors: lan l. Hear Res. 2016 May;335:53-63. doi: 10.1016/j.heares.2016.01.008. Epub 2016 Jan 15. Hear Res. 2016. PMID: 26778470
Unilateral auditory neuropathy spectrum disorder.
Zhang QJ, Lan L, Shi W, Wang DY, Qi Y, Zong L, Li Q, Wang H, Ding HN, Li N, Han B, Wang QJ. Zhang QJ, et al. Among authors: lan l. Acta Otolaryngol. 2012 Jan;132(1):72-9. doi: 10.3109/00016489.2011.629630. Epub 2011 Nov 10. Acta Otolaryngol. 2012. PMID: 22073929
SIX2 haploinsufficiency causes conductive hearing loss with ptosis in humans.
Guan J, Wang D, Cao W, Zhao Y, Du R, Yuan H, Liu Q, Lan L, Zong L, Yang J, Yin Z, Han B, Zhang F, Wang Q. Guan J, et al. Among authors: lan l. J Hum Genet. 2016 Nov;61(11):917-922. doi: 10.1038/jhg.2016.86. Epub 2016 Jul 7. J Hum Genet. 2016. PMID: 27383657 Free PMC article.
Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder.
Zong L, Guan J, Ealy M, Zhang Q, Wang D, Wang H, Zhao Y, Shen Z, Campbell CA, Wang F, Yang J, Sun W, Lan L, Ding D, Xie L, Qi Y, Lou X, Huang X, Shi Q, Chang S, Xiong W, Yin Z, Yu N, Zhao H, Wang J, Wang J, Salvi RJ, Petit C, Smith RJ, Wang Q. Zong L, et al. Among authors: lan l. J Med Genet. 2015 Aug;52(8):523-31. doi: 10.1136/jmedgenet-2014-102961. Epub 2015 May 18. J Med Genet. 2015. PMID: 25986071 Free PMC article.
19 results