| 1 | DFNB99, TMEM132E
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| Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
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| Liaqat K, Hussain S, Bilal M, Nasir A, Acharya A, Ali RH, Nawaz S, Umair M, Schrauwen I, Ahmad W, Leal SM
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| J Hum Genet. Jan;65(2):187-192. doi: 10.1038/s10038-019-0691-4. Epub 2019 Oct 28. Erratum in: J Hum Genet. 2022 Mar;67(3):181. 2022
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| 2 | DFNB99, TMEM132E
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| Further evidence of involvement of TMEM132E in autosomal recessive nonsyndromic hearing impairment
|
| Liaqat K, Hussain S, Bilal M, Nasir A, Acharya A, Ali RH, Nawaz S, Umair M, Schrauwen I, Ahmad W, Leal SM.
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| J Hum Genet. Jan;65(2):187-192. doi: 10.1038/s10038-019-0691-4. Epub 2019 Oct 28. Erratum in: J Hum Genet. 2022 Mar;67(3):181. 2020
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| 3 | DFNB99, TMEM132E
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| Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99
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| Li J, Zhao X, Xin Q, Shan S, Jiang B, Jin Y, Yuan H, Dai P, Xiao R, Zhang Q, Xiao J, Shao C, Gong Y, Liu Q
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| Hum Mutat. Jan;36(1):98-105. doi: 10.1002/humu.22712. Epub 2014 Nov 28 2015
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