PubMed for id: 332110

Year	Number of Results
1997	1
2003	2
2005	2
2006	3
2007	1
2008	4
2009	5
2010	1
2011	3
2012	3
2013	1
2014	3
2015	3
2016	2
2017	1
2018	2
2019	4
2020	4
2022	4
2024	0

1

Novel mutation located in EC7 domain of protocadherin-15 uncovered by targeted massively parallel sequencing in a family segregating non-syndromic deafness DFNB23.

Zhan Y, Liu M, Chen D, Chen K, Jiang H. Zhan Y, et al. Int J Pediatr Otorhinolaryngol. 2015 Jul;79(7):983-6. doi: 10.1016/j.ijporl.2015.04.002. Epub 2015 Apr 11. Int J Pediatr Otorhinolaryngol. 2015. PMID: 25930172

2

Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.

Ammar-Khodja F, Faugère V, Baux D, Giannesini C, Léonard S, Makrelouf M, Malek R, Djennaoui D, Zenati A, Claustres M, Roux AF. Ammar-Khodja F, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):174-9. doi: 10.1016/j.ejmg.2009.03.018. Epub 2009 Apr 16. Eur J Med Genet. 2009. PMID: 19375528

3

Gene structure and mutant alleles of PCDH15: nonsyndromic deafness DFNB23 and type 1 Usher syndrome.

Ahmed ZM, Riazuddin S, Aye S, Ali RA, Venselaar H, Anwar S, Belyantseva PP, Qasim M, Riazuddin S, Friedman TB. Ahmed ZM, et al. Hum Genet. 2008 Oct;124(3):215-23. doi: 10.1007/s00439-008-0543-3. Epub 2008 Aug 22. Hum Genet. 2008. PMID: 18719945 Free PMC article.

4

PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23.

Ahmed ZM, Riazuddin S, Ahmad J, Bernstein SL, Guo Y, Sabar MF, Sieving P, Riazuddin S, Griffith AJ, Friedman TB, Belyantseva IA, Wilcox ER. Ahmed ZM, et al. Hum Mol Genet. 2003 Dec 15;12(24):3215-23. doi: 10.1093/hmg/ddg358. Epub 2003 Oct 21. Hum Mol Genet. 2003. PMID: 14570705

5

Mutation screening of the PCDH15 gene in Spanish patients with Usher syndrome type I.

Jaijo T, Oshima A, Aller E, Carney C, Usami S, Millán JM, Kimberling WJ. Jaijo T, et al. Mol Vis. 2012;18:1719-26. Epub 2012 Jun 23. Mol Vis. 2012. PMID: 22815625 Free PMC article.

6

Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15.

Doucette L, Merner ND, Cooke S, Ives E, Galutira D, Walsh V, Walsh T, MacLaren L, Cater T, Fernandez B, Green JS, Wilcox ER, Shotland LI, Li XC, Lee M, King MC, Young TL. Doucette L, et al. Eur J Hum Genet. 2009 May;17(5):554-64. doi: 10.1038/ejhg.2008.231. Epub 2008 Dec 24. Eur J Hum Genet. 2009. PMID: 19107147 Free PMC article.

7

Development of outer hair cells in Ames waltzer mice: mutation in protocadherin 15 affects development of cuticular plate and associated structures.

Kikkawa YS, Pawlowski KS, Wright CG, Alagramam KN. Kikkawa YS, et al. Anat Rec (Hoboken). 2008 Feb;291(2):224-32. doi: 10.1002/ar.20632. Anat Rec (Hoboken). 2008. PMID: 18085631 Free article.

8

The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15.

Ahmed ZM, Goodyear R, Riazuddin S, Lagziel A, Legan PK, Behra M, Burgess SM, Lilley KS, Wilcox ER, Riazuddin S, Griffith AJ, Frolenkov GI, Belyantseva IA, Richardson GP, Friedman TB. Ahmed ZM, et al. J Neurosci. 2006 Jun 28;26(26):7022-34. doi: 10.1523/JNEUROSCI.1163-06.2006. J Neurosci. 2006. PMID: 16807332 Free PMC article.

9

ARNSHL gene identification: past, present and future.

Imtiaz A. Imtiaz A. Mol Genet Genomics. 2022 Sep;297(5):1185-1193. doi: 10.1007/s00438-022-01926-x. Epub 2022 Jul 23. Mol Genet Genomics. 2022. PMID: 35869994 Review.

10

Template-independent genome editing in the Pcdh15^av-3j mouse, a model of human DFNB23 nonsyndromic deafness.

Liu L, Zou L, Li K, Hou H, Hu Q, Liu S, Li J, Song C, Chen J, Wang S, Wang Y, Li C, Du H, Li JL, Chen F, Xu Z, Sun W, Sun Q, Xiong W. Liu L, et al. Cell Rep. 2022 Jul 12;40(2):111061. doi: 10.1016/j.celrep.2022.111061. Cell Rep. 2022. PMID: 35830793 Free article.

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