| 1 | DFNA15, POU4F3
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| A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.
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| Lee HK, Park HJ, Lee KY, Park R, Kim UK.
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| Biochem Biophys Res Commun 396(3):626-30. Epub 2010 Apr 29. Erratum in: Biochem Biophys Res Commun. 2010 Aug 6;398(4):790. PMID: 20434433 2010
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| 2 | DFNA15, POU4F3
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| Mild and variable audiometric and vestibular features in a third DFNA15 family with a novel mutation in POU4F3.
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| de Heer AM, Huygen PL, Collin RW, Kremer H, Cremers CW.
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| Ann Otol Rhinol Laryngol 118(4):313-20.
2009
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| 3 | POU4F3, DFNA15
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| Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.
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| Collin RW, Chellappa R, Pauw RJ, Vriend G, Oostrik J, van Drunen W, Huygen PL, Admiraal R, Hoefsloot LH, Cremers FP, Xiang M, Cremers CW, Kremer H.
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| Hum Mutat 29(4):545-54. 2008
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| 4 | DFNA15, POU4F3
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| Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.
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| Pauw RJ, van Drunen FJ, Collin RW, Huygen PL, Kremer H, Cremers CW.
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| Arch Otolaryngol Head Neck Surg 134(3):294-300.PMID: 18347256 2008
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| 5 | DFNA15, POU4F3
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| Molecular modelling insights into DFNA15 mediated enhancement of POU4F3 stability.
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| Frenz CM, Lefebvre PP.
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| Int J Comput Biol Drug Des 1(3):295-301.
2008
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| 6 | POU4F3, DFNA15
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| Identification and functional analysis of common sequence variants in the DFNA15 gene, Brn-3c.
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| Nolan LS, Jagutpal SS, Cadge BA, Woo P, Dawson SJ.
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| Gene 400(1-2):89-97. Epub 2007 Jun 12. 2007
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| 7 | DFNA15, POU4F3
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| Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.
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| Vahava O, et al.
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| Science 279 : 1950-1953. 1998
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