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

Year Number of Results
1994 1
1995 1
1996 1
1997 1
1999 1
2000 1
2001 2
2002 1
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2004 3
2005 1
2023 0

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PubMed (OMIM) for id: 419894

15 results

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Page 1
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.
Myosin VI is a processive motor with a large step size.
Rock RS, Rice SE, Wells AL, Purcell TJ, Spudich JA, Sweeney HL. Rock RS, et al. Proc Natl Acad Sci U S A. 2001 Nov 20;98(24):13655-9. doi: 10.1073/pnas.191512398. Epub 2001 Nov 13. Proc Natl Acad Sci U S A. 2001. PMID: 11707568 Free PMC article.
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.
Melchionda S, Ahituv N, Bisceglia L, Sobe T, Glaser F, Rabionet R, Arbones ML, Notarangelo A, Di Iorio E, Carella M, Zelante L, Estivill X, Avraham KB, Gasparini P. Melchionda S, et al. Am J Hum Genet. 2001 Sep;69(3):635-40. doi: 10.1086/323156. Epub 2001 Jul 20. Am J Hum Genet. 2001. PMID: 11468689 Free PMC article.
15 results