RecName: Full=POU domain, class 4, transcription factor 3

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A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss. [Sci Rep. 2017]
A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss.
Lin YH, Lin YH, Lu YC, Liu TC, Chen CY, Hsu CJ, Chen PL, Wu CC. Sci Rep. 2017 Aug 8; 7(1):7551. Epub 2017 Aug 8.
Brn3c null mutant mice show long-term, incomplete retention of some afferent inner ear innervation. [BMC Neurosci. 2003]
Brn3c null mutant mice show long-term, incomplete retention of some afferent inner ear innervation.
Xiang M, Maklad A, Pirvola U, Fritzsch B. BMC Neurosci. 2003 Jan 30; 4:2. Epub 2003 Jan 30.
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. [Science. 1998]
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.
Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, et al. Science. 1998 Mar 20; 279(5358):1950-4.

RefSeq protein
See the reference protein sequence for POU domain, class 4, transcription factor 3 (NP_001102359.1).

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RecName: Full=POU domain, class 4, transcription factor 3
RecName: Full=POU domain, class 4, transcription factor 3
gi|1100163517|sp|D3ZTL1.1|PO4F3_RAT

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