| 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 | TMEM132A, TMEM132B, TMEM132C, TMEM132D, TMEM132E
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| The C. elegans homolog of human panic-disorder risk gene TMEM132D orchestrates neuronal morphogenesis through the WAVE-regulatory complex.
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| Wang X, Jiang W, Luo S, Yang X, Wang C, Wang B, Dang Y, Shen Y, Ma DK.
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| Mol Brain. Mar 16;14(1):54. doi: 10.1186/s13041-021-00767-w. 2021
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| 3 | 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. 2020
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| 4 | TMEM132A, TMEM132B, TMEM132C, TMEM132D, TMEM132E
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| TMEM132: an ancient architecture of cohesin and immunoglobulin domains define a new family of neural adhesion molecules
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| Sanchez-Pulido L, Ponting CP.
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| Bioinformatics. Mar 1;34(5):721-724. doi: 10.1093/bioinformatics/btx689. 2018
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| 5 | 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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