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

Year Number of Results
1994 1
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2008 2
2009 1
2011 1
2013 2
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2015 3
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2017 3
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PubMed for id: 375076

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Page 1
A novel splice site mutation of myosin VI in mice leads to stereociliary fusion caused by disruption of actin networks in the apical region of inner ear hair cells.
Seki Y, Miyasaka Y, Suzuki S, Wada K, Yasuda SP, Matsuoka K, Ohshiba Y, Endo K, Ishii R, Shitara H, Kitajiri SI, Nakagata N, Takebayashi H, Kikkawa Y. Seki Y, et al. PLoS One. 2017 Aug 23;12(8):e0183477. doi: 10.1371/journal.pone.0183477. eCollection 2017. PLoS One. 2017. PMID: 28832620 Free PMC article.
Mutations of MYO6 are associated with recessive deafness, DFNB37.
Ahmed ZM, Morell RJ, Riazuddin S, Gropman A, Shaukat S, Ahmad MM, Mohiddin SA, Fananapazir L, Caruso RC, Husnain T, Khan SN, Riazuddin S, Griffith AJ, Friedman TB, Wilcox ER. Ahmed ZM, et al. Am J Hum Genet. 2003 May;72(5):1315-22. doi: 10.1086/375122. Epub 2003 Apr 8. Am J Hum Genet. 2003. PMID: 12687499 Free PMC article.
23 results