1. Du, Qiang, Sun, Qin, Gu, Xiaodong, Guo, Luo, Li, Huawei. 2022. Novel homozygous variant in the PDZD7 gene in a family with nonsyndromic sensorineural hearing loss. In BMC medical genomics, 15, 135. doi:10.1186/s12920-022-01289-7. https://pubmed.ncbi.nlm.nih.gov/35715776/
2. Vona, Barbara, Lechno, Stanislav, Hofrichter, Michaela A H, Zechner, Ulrich, Bartsch, Oliver. . Confirmation of PDZD7 as a Nonsyndromic Hearing Loss Gene. In Ear and hearing, 37, e238-46. doi:10.1097/AUD.0000000000000278. https://pubmed.ncbi.nlm.nih.gov/26849169/
3. Du, Haibo, Ren, Rui, Chen, Panpan, Xu, Zhigang, Wang, Yanfei. 2018. Identification of Binding Partners of Deafness-Related Protein PDZD7. In Neural plasticity, 2018, 2062346. doi:10.1155/2018/2062346. https://pubmed.ncbi.nlm.nih.gov/29796015/
4. Du, Haibo, Zou, Linzhi, Ren, Rui, Xiong, Wei, Xu, Zhigang. 2019. Lack of PDZD7 long isoform disrupts ankle-link complex and causes hearing loss in mice. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34, 1136-1149. doi:10.1096/fj.201901657RR. https://pubmed.ncbi.nlm.nih.gov/31914662/
5. Guan, Jing, Wang, Hongyang, Lan, Lan, Wang, Dayong, Wang, Qiuju. 2017. Novel recessive PDZD7 biallelic mutations in two Chinese families with non-syndromic hearing loss. In American journal of medical genetics. Part A, 176, 99-106. doi:10.1002/ajmg.a.38477. https://pubmed.ncbi.nlm.nih.gov/29048736/
智鼠故事 
