1. Zhang, Lang, Yang, Jin-Yuan, Wang, Qiu-Quan, Huang, Sha-Sha, Yuan, Yong-Yi. 2024. MPZL2-a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population. In BMC medical genomics, 17, 32. doi:10.1186/s12920-023-01786-3. https://pubmed.ncbi.nlm.nih.gov/38254107/
2. Jiang, Luoying, Hu, Shao Wei, Wang, Zijing, He, Yingzi, Shu, Yilai. 2024. Hearing restoration by gene replacement therapy for a multisite-expressed gene in a mouse model of human DFNB111 deafness. In American journal of human genetics, 111, 2253-2264. doi:10.1016/j.ajhg.2024.08.008. https://pubmed.ncbi.nlm.nih.gov/39241775/
3. Bademci, Guney, Abad, Clemer, Incesulu, Armagan, Walz, Katherina, Tekin, Mustafa. 2018. MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss. In Human genetics, 137, 479-486. doi:10.1007/s00439-018-1901-4. https://pubmed.ncbi.nlm.nih.gov/29982980/
4. Li, Weitao, Guo, Luo, Chen, Bing, Shu, Yilai, Li, Huawei. 2023. MPZL2 variant analysis with whole exome sequencing in a cohort of Chinese hearing loss patients. In International journal of pediatric otorhinolaryngology, 171, 111635. doi:10.1016/j.ijporl.2023.111635. https://pubmed.ncbi.nlm.nih.gov/37390746/
5. Wesdorp, Mieke, Murillo-Cuesta, Silvia, Peters, Theo, Pennings, Ronald J E, Kremer, Hannie. 2018. MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse. In American journal of human genetics, 103, 74-88. doi:10.1016/j.ajhg.2018.05.011. https://pubmed.ncbi.nlm.nih.gov/29961571/
6. Wang, Zhili, Jiang, Mengda, Wu, Hao, Li, Yun, Chen, Ying. 2022. A novel MPZL2 c.68delC variant is associated with progressive hearing loss in Chinese population and literature review. In Laryngoscope investigative otolaryngology, 7, 870-876. doi:10.1002/lio2.829. https://pubmed.ncbi.nlm.nih.gov/35734045/