1. Bernardinelli, Emanuele, Huber, Florian, Roesch, Sebastian, Dossena, Silvia. 2023. Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review. In Biomedicines, 11, . doi:10.3390/biomedicines11061695. https://pubmed.ncbi.nlm.nih.gov/37371790/
2. Defourny, Jean. 2022. Considering gene therapy to protect from X-linked deafness DFNX2 and associated neurodevelopmental disorders. In Ibrain, 8, 431-441. doi:10.1002/ibra.12068. https://pubmed.ncbi.nlm.nih.gov/37786584/
3. Dang, Jiong, Bian, Panpan, Chen, Chao, Guan, Minxin, Guo, Yufen. 2025. Impact of POU3F4 mutation on cochlear development and auditory function. In Cell communication and signaling : CCS, 23, 121. doi:10.1186/s12964-025-02133-y. https://pubmed.ncbi.nlm.nih.gov/40045370/
4. Raft, Steven, Coate, Thomas M, Kelley, Matthew W, Crenshaw, E Bryan, Wu, Doris K. 2014. Pou3f4-mediated regulation of ephrin-b2 controls temporal bone development in the mouse. In PloS one, 9, e109043. doi:10.1371/journal.pone.0109043. https://pubmed.ncbi.nlm.nih.gov/25299585/
5. Yu, Rong, Wang, Kai, Xiong, Yuanping, Jiang, Hongqun. 2022. A novel mutation of X-linked recessive deafness gene POU3F4 in a boy with congenital deafness. In Laryngoscope investigative otolaryngology, 7, 1150-1154. doi:10.1002/lio2.850. https://pubmed.ncbi.nlm.nih.gov/36000053/
6. Bernardinelli, Emanuele, Roesch, Sebastian, Simoni, Edi, Sarikas, Antonio, Dossena, Silvia. 2022. Novel POU3F4 variants identified in patients with inner ear malformations exhibit aberrant cellular distribution and lack of SLC6A20 transcriptional upregulation. In Frontiers in molecular neuroscience, 15, 999833. doi:10.3389/fnmol.2022.999833. https://pubmed.ncbi.nlm.nih.gov/36245926/