Homo sapiens POU class 4 homeobox 3 (POU4F3), RefSeqGene (LRG_1355) on - Nucleotide

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Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects. [Sci Rep. 2023]
Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.
Lee SY, Kim MY, Han JH, Park SS, Yun Y, Jee SC, Han JJ, Lee JH, Seok H, Choi BY. Sci Rep. 2023 Aug 3; 13(1):12584. Epub 2023 Aug 3.
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses. [Eur J Hum Genet. 2023]
Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses.
Singh S, Penney C, Griffin A, Woodland G, Werdyani S, Benteau TA, Abdelfatah N, Squires J, King B, Houston J, et al. Eur J Hum Genet. 2023 Jul; 31(7):815-823. Epub 2023 Apr 19.
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers. [Elife. 2022]
The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.
Oravcová M, Nie M, Zilio N, Maeda S, Jami-Alahmadi Y, Lazzerini-Denchi E, Wohlschlegel JA, Ulrich HD, Otomo T, Boddy MN. Elife. 2022 Nov 14; 11. Epub 2022 Nov 14.

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Nucleotide