PubMed for id: 481290

Year	Number of Results
2001	1
2003	1
2004	1
2005	1
2010	4
2011	2
2012	4
2013	3
2014	1
2015	2
2016	2
2017	5
2018	2
2019	1
2020	3
2021	2
2024	0

1

Phenotypic variability of CLDN14 mutations causing DFNB29 hearing loss in the Pakistani population.

Bashir ZE, Latief N, Belyantseva IA, Iqbal F, Riazuddin SA, Khan SN, Friedman TB, Riazuddin S, Riazuddin S. Bashir ZE, et al. J Hum Genet. 2013 Feb;58(2):102-8. doi: 10.1038/jhg.2012.143. Epub 2012 Dec 13. J Hum Genet. 2013. PMID: 23235333 Free PMC article.

2

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB. Ben-Yosef T, et al. Hum Mol Genet. 2003 Aug 15;12(16):2049-61. doi: 10.1093/hmg/ddg210. Hum Mol Genet. 2003. PMID: 12913076

3

Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29.

Wilcox ER, Burton QL, Naz S, Riazuddin S, Smith TN, Ploplis B, Belyantseva I, Ben-Yosef T, Liburd NA, Morell RJ, Kachar B, Wu DK, Griffith AJ, Riazuddin S, Friedman TB. Wilcox ER, et al. Cell. 2001 Jan 12;104(1):165-72. doi: 10.1016/s0092-8674(01)00200-8. Cell. 2001. PMID: 11163249 Free article.

4

Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant.

Kitano T, Kitajiri SI, Nishio SY, Usami SI. Kitano T, et al. Int J Mol Sci. 2019 Sep 16;20(18):4579. doi: 10.3390/ijms20184579. Int J Mol Sci. 2019. PMID: 31527509 Free PMC article.

5

Diverse pattern of gap junction beta-2 and gap junction beta-4 genes mutations and lack of contribution of DFNB21, DFNB24, DFNB29, and DFNB42 loci in autosomal recessive nonsyndromic hearing loss patients in Hormozgan, Iran.

Laleh MA, Naseri M, Zonouzi AAP, Zonouzi AP, Masoudi M, Ahangari N, Shams L, Nejatizadeh A. Laleh MA, et al. J Res Med Sci. 2017 Aug 16;22:99. doi: 10.4103/jrms.JRMS_976_16. eCollection 2017. J Res Med Sci. 2017. PMID: 28900455 Free PMC article.

6

A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect.

Pater JA, Benteau T, Griffin A, Penney C, Stanton SG, Predham S, Kielley B, Squires J, Zhou J, Li Q, Abdelfatah N, O'Rielly DD, Young TL. Pater JA, et al. Hum Genet. 2017 Jan;136(1):107-118. doi: 10.1007/s00439-016-1746-7. Epub 2016 Nov 12. Hum Genet. 2017. PMID: 27838790 Free PMC article.

7

Molecular Distribution of Deafness Loci in Various Ethnic Groups of the Punjab, Pakistan.

Ullah S, Aslamkhan M, Rasheed A. Ullah S, et al. J Coll Physicians Surg Pak. 2015 Aug;25(8):573-8. J Coll Physicians Surg Pak. 2015. PMID: 26305302

8

Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss.

Kim MA, Kim YR, Sagong B, Cho HJ, Bae JW, Kim J, Lee J, Park HJ, Choi JY, Lee KY, Kim UK. Kim MA, et al. PLoS One. 2014 Apr 21;9(4):e95646. doi: 10.1371/journal.pone.0095646. eCollection 2014. PLoS One. 2014. PMID: 24752540 Free PMC article.

9

Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.

Charif M, Boulouiz R, Bakhechane A, Benrahma H, Nahili H, Eloualid A, Rouba H, Kandil M, Abidi O, Lenaers G, Barakat A. Charif M, et al. Indian J Hum Genet. 2013 Jul;19(3):331-6. doi: 10.4103/0971-6866.120828. Indian J Hum Genet. 2013. PMID: 24339547 Free PMC article.

10

Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.

Charif M, Bakhchane A, Abidi O, Boulouiz R, Eloualid A, Roky R, Rouba H, Kandil M, Lenaers G, Barakat A. Charif M, et al. Gene. 2013 Jul 1;523(1):103-5. doi: 10.1016/j.gene.2013.03.123. Epub 2013 Apr 13. Gene. 2013. PMID: 23590985 Free article.

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