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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
1995 3
1996 2
1998 6
1999 7
2000 4
2001 3
2002 2
2003 4
2004 2
2005 4
2006 6
2007 6
2008 3
2009 6
2010 8
2011 6
2012 4
2013 3
2014 8
2015 8
2016 9
2017 6
2018 7
2019 13
2020 6
2021 8
2022 11
2023 3

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PubMed for id: 325373

138 results

Results by year

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Page 1
[Analysis of MYO15A variation in children with DFNB3].
Ren SM, Wu QH, Jiao ZH, Chen YB, Chen C, Kong XD, Qin ZB. Ren SM, et al. Zhonghua Er Ke Za Zhi. 2020 Oct 2;58(10):818-823. doi: 10.3760/cma.j.cn112140-20200220-00115. Zhonghua Er Ke Za Zhi. 2020. PMID: 32987461 Chinese.
Mutational Spectrum of MYO15A and the Molecular Mechanisms of DFNB3 Human Deafness.
Rehman AU, Bird JE, Faridi R, Shahzad M, Shah S, Lee K, Khan SN, Imtiaz A, Ahmed ZM, Riazuddin S, Santos-Cortez RL, Ahmad W, Leal SM, Riazuddin S, Friedman TB. Rehman AU, et al. Hum Mutat. 2016 Oct;37(10):991-1003. doi: 10.1002/humu.23042. Epub 2016 Aug 21. Hum Mutat. 2016. PMID: 27375115 Free PMC article.
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.
Belguith H, Aifa-Hmani M, Dhouib H, Said MB, Mosrati MA, Lahmar I, Moalla J, Charfeddine I, Driss N, Arab SB, Ghorbel A, Ayadi H, Masmoudi S. Belguith H, et al. Genet Test Mol Biomarkers. 2009 Feb;13(1):147-51. doi: 10.1089/gtmb.2008.0077. Genet Test Mol Biomarkers. 2009. PMID: 19309289
MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation.
Kalay E, Uzumcu A, Krieger E, Caylan R, Uyguner O, Ulubil-Emiroglu M, Erdol H, Kayserili H, Hafiz G, Başerer N, Heister AJ, Hennies HC, Nürnberg P, Başaran S, Brunner HG, Cremers CW, Karaguzel A, Wollnik B, Kremer H. Kalay E, et al. Am J Med Genet A. 2007 Oct 15;143A(20):2382-9. doi: 10.1002/ajmg.a.31937. Am J Med Genet A. 2007. PMID: 17853461
138 results