| 1 | DFNA10, DFNA12, DFNA13, DFNA44, DFNA8
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| Research progress in pathogenic genes of hereditary non-syndromic mid-frequency deafness.
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| Xia W, Liu F, Ma D.
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| Front Med 10(2):137-42. doi: 10.1007/s11684-016-0449-8. Epub 2016 May 3. Review.
2016
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| 2 | DFNA10, EYA4
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| Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.
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| Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ.
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| Am J Med Genet A 143(14):1592-8. 2007
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| 3 | DFNA10, EYA4
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| A novel splice site mutation in EYA4 causes DFNA10 hearing loss.
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| Hildebrand MS, Coman D, Yang T, Gardner RJ, Rose E, Smith RJ, Bahlo M, Dahl HH.
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| Am J Med Genet A 143(14):1599-604. 2007
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| 4 | EYA4, DFNA10
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| A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10.
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| Pfister M, Toth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nurnberg P, Kupka S.
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| Mol Med 8(10):607-11. 2002
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| 5 | DFNA10, EYA4
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| Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
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| Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, Tranebjarg L, Morton CC, Ryan AF, Van Camp G, Smith RJ.
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| Hum Mol Genet 10(3):195-200. 2001
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| 6 | DFNA10
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| Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
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| Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjarg L, Smith RJ, Van Camp G.
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| Hum Genet 107(1):7-11. 2000
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| 7 | 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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| 8 | DFNA10
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| A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.
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| O'Neill ME, et al.
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| Hum Mol Genet 5 : 853-856. 1996
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