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Comment
. 2009 Mar;75(3):227-9.
doi: 10.1111/j.1399-0004.2009.01150_3.x.

LRTOMT: a new tone in understanding the symphony of non-syndromic deafness

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Comment

LRTOMT: a new tone in understanding the symphony of non-syndromic deafness

J M Schulze. Clin Genet. 2009 Mar.
No abstract available

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Comment on

  • Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
    Ahmed ZM, Masmoudi S, Kalay E, Belyantseva IA, Mosrati MA, Collin RW, Riazuddin S, Hmani-Aifa M, Venselaar H, Kawar MN, Tlili A, van der Zwaag B, Khan SY, Ayadi L, Riazuddin SA, Morell RJ, Griffith AJ, Charfedine I, Caylan R, Oostrik J, Karaguzel A, Ghorbel A, Riazuddin S, Friedman TB, Ayadi H, Kremer H. Ahmed ZM, et al. Nat Genet. 2008 Nov;40(11):1335-40. doi: 10.1038/ng.245. Epub 2008 Oct 26. Nat Genet. 2008. PMID: 18953341 Free PMC article.

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