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

Year Number of Results
2004 1
2005 2
2010 1
2011 1
2012 2
2013 2
2014 5
2015 4
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2017 3
2018 2
2019 1
2023 1
2024 0

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PubMed for id: 351225

25 results

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Page 1
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.
Ildr1b is essential for semicircular canal development, migration of the posterior lateral line primordium and hearing ability in zebrafish: implications for a role in the recessive hearing impairment DFNB42.
Sang Q, Zhang J, Feng R, Wang X, Li Q, Zhao X, Xing Q, Chen W, Du J, Sun S, Chai R, Liu D, Jin L, He L, Li H, Wang L. Sang Q, et al. Hum Mol Genet. 2014 Dec 1;23(23):6201-11. doi: 10.1093/hmg/ddu340. Epub 2014 Jul 2. Hum Mol Genet. 2014. PMID: 24990150
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, Shearer AE, Ahmad A, Kahrizi K, Shaikh RS, Ali RA, Khan SN, Goebel I, Meyer NC, Kimberling WJ, Webster JA, Stephan DA, Schiller MR, Bahlo M, Najmabadi H, Gillespie PG, Nürnberg P, Wollnik B, Riazuddin S, Smith RJ, Ahmad W, Müller U, Hammerschmidt M, Friedman TB, Riazuddin S, Leal SM, Ahmad J, Kubisch C. Borck G, et al. Am J Hum Genet. 2011 Feb 11;88(2):127-37. doi: 10.1016/j.ajhg.2010.12.011. Epub 2011 Jan 20. Am J Hum Genet. 2011. PMID: 21255762 Free PMC article.
25 results