PubMed for id: 322209

Year	Number of Results
1995	1
1998	3
2000	3
2001	2
2002	1
2004	3
2005	1
2008	1
2010	2
2011	2
2012	1
2015	2
2016	1
2020	1
2024	0

1

Genetic heterogeneity of deafness phenotypes linked to DFNA4.

Yang T, Pfister M, Blin N, Zenner HP, Pusch CM, Smith RJ. Yang T, et al. Am J Med Genet A. 2005 Nov 15;139(1):9-12. doi: 10.1002/ajmg.a.30989. Am J Med Genet A. 2005. PMID: 16222661

2

Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33.

Pusch CM, Meyer B, Kupka S, Smith RJ, Lalwani AK, Zenner HP, Blin N, Nürnberg P, Pfister M. Pusch CM, et al. J Mol Med (Berl). 2004 Jun;82(6):398-402. doi: 10.1007/s00109-004-0538-z. Epub 2004 Mar 24. J Mol Med (Berl). 2004. PMID: 15042303

3

Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).

Donaudy F, Snoeckx R, Pfister M, Zenner HP, Blin N, Di Stazio M, Ferrara A, Lanzara C, Ficarella R, Declau F, Pusch CM, Nürnberg P, Melchionda S, Zelante L, Ballana E, Estivill X, Van Camp G, Gasparini P, Savoia A. Donaudy F, et al. Am J Hum Genet. 2004 Apr;74(4):770-6. doi: 10.1086/383285. Epub 2004 Mar 10. Am J Hum Genet. 2004. PMID: 15015131 Free PMC article.

4

Genomic structure, cochlear expression, and mutation screening of KCNK6, a candidate gene for DFNA4.

Mhatre AN, Li J, Chen AF, Yost CS, Smith RJ, Kindler CH, Lalwani AK. Mhatre AN, et al. J Neurosci Res. 2004 Jan 1;75(1):25-31. doi: 10.1002/jnr.10839. J Neurosci Res. 2004. PMID: 14689445

5

Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.

Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, König E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N. Mirghomizadeh F, et al. Eur J Hum Genet. 2002 Feb;10(2):95-9. doi: 10.1038/sj.ejhg.5200769. Eur J Hum Genet. 2002. PMID: 11938438

6

2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4.

Bearer EL, Chen AF, Chen AH, Li Z, Mark HF, Smith RJ, Jackson CL. Bearer EL, et al. Ann Hum Genet. 2000 May;64(Pt 3):189-96. doi: 10.1046/j.1469-1809.2000.6430189.x. Ann Hum Genet. 2000. PMID: 11409409 Free PMC article.

7

Novel coding-region polymorphisms in mitochondrial seryl-tRNA synthetase (SARSM) and mitoribosomal protein S12 (RPMS12) genes in DFNA4 autosomal dominant deafness families.

Shah ZH, Toompuu M, Hakkinen T, Rovio AT, van Ravenswaay C, De Leenheer EM, Smith RJ, Cremers FP, Cremers CW, Jacobs HT. Shah ZH, et al. Hum Mutat. 2001 May;17(5):433-4. doi: 10.1002/humu.1123. Hum Mutat. 2001. PMID: 11317363

8

A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss.

Wang M, Zhou Y, Zhang F, Fan Z, Bai X, Wang H. Wang M, et al. BMC Med Genet. 2020 Jul 25;21(1):154. doi: 10.1186/s12881-020-01086-y. BMC Med Genet. 2020. PMID: 32711451 Free PMC article.

9

Loss of Myh14 Increases Susceptibility to Noise-Induced Hearing Loss in CBA/CaJ Mice.

Fu X, Zhang L, Jin Y, Sun X, Zhang A, Wen Z, Zhou Y, Xia M, Gao J. Fu X, et al. Neural Plast. 2016;2016:6720420. doi: 10.1155/2016/6720420. Epub 2016 Dec 22. Neural Plast. 2016. PMID: 28101381 Free PMC article.

10

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y. Wang H, et al. J Hum Genet. 2015 Mar;60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15. J Hum Genet. 2015. PMID: 25589040 Free PMC article.

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