| 1 | MYH14, DFNA4
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| Genetic heterogeneity of deafness phenotypes linked to DFNA4.
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| Yang T, Pfister M, Blin N, Zenner HP, Pusch CM, Smith RJ.
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| Am J Med Genet A 139(1):9-12. 2005
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| 2 | MYH14, DFNA4
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| Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).
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| Donaudy F, Snoeckx R, Pfister M, Zenner HP, Blin N, Di Stazio M, Ferrara A, Lanzara C, Ficarella R, Declau F, Pusch CM, Nurnberg P, Melchionda S, Zelante L, Ballana E, Estivill X, Van Camp G, Gasparini P, Savoia A.
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| Am J Hum Genet 74(4):770-6. Epub 2004 Mar 10. 2004
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| 3 | DFNA4
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| Refinement of the DFNA4 locus to a 1.44 Mb region in 19q13.33.
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| Pusch CM, Meyer B, Kupka S, Smith RJ, Lalwani AK, Zenner HP, Blin N, Nurnberg P, Pfister M.
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| J Mol Med 82(6):398-402. Epub 2004 Mar 24. 2004
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| 4 | DFNA4
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| Second family with hearing impairment linked to 19q13 and refined DFNA4 localisation.
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| Mirghomizadeh F, Bardtke B, Devoto M, Pfister M, Oeken J, Konig E, Vitale E, Riccio A, De Rienzo A, Zenner HP, Blin N.
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| Eur J Hum Genet 10(2):95-9. 2002
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| 5 | DFN2, DFNA10, DFNA13, DFNA18, DFNA2, DFNA4, DFNA5, DFNA6, DFNB12, DFNB13, DFNB15, DFNB16, DFNB17, DFNB19, DFNB6, DFNB7, DFNB8, USH1D, USH1E, USH1F, CLRN1
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| Human cochlear expressed sequence tags provide insight into cochlear gene expression and identify candidate genes for deafness.
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| Skvorak AB, et al.
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| Hum Mol Genet 8(3):439-52 1999
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| 6 | DFNA4
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| Linkage of a gene for dominant non-syndromic deafness to chromosome 19.
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| Chen AH, et al.
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| Hum Mol Genet 4 : 1073-1076. 1995
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