1. Mehregan, Hoda, Mohseni, Marzieh, Akbari, Mojdeh, Kahrizi, Kimia, Najmabadi, Hossein. 2019. Novel Mutations in KCNQ4, LHFPL5 and COCH Genes in Iranian Families with Hearing Impairment. In Archives of Iranian medicine, 22, 189-197. doi:. https://pubmed.ncbi.nlm.nih.gov/31126177/
2. Kalay, Ersan, Li, Yun, Uzumcu, Abdullah, Kremer, Hannie, Wollnik, Bernd. . Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing loss. In Human mutation, 27, 633-9. doi:. https://pubmed.ncbi.nlm.nih.gov/16752389/
3. Yu, Xiaojie, Zhao, Qirui, Li, Xiaofen, Xiong, Wei, Huang, Pingbo. 2020. Deafness mutation D572N of TMC1 destabilizes TMC1 expression by disrupting LHFPL5 binding. In Proceedings of the National Academy of Sciences of the United States of America, 117, 29894-29903. doi:10.1073/pnas.2011147117. https://pubmed.ncbi.nlm.nih.gov/33168709/
4. Liaqat, Khurram, Chiu, Ilene, Lee, Kwanghyuk, Ahmad, Wasim, Leal, Suzanne M. 2018. Novel missense and 3'-UTR splice site variants in LHFPL5 cause autosomal recessive nonsyndromic hearing impairment. In Journal of human genetics, 63, 1099-1107. doi:10.1038/s10038-018-0502-3. https://pubmed.ncbi.nlm.nih.gov/30177809/
5. György, Bence, Sage, Cyrille, Indzhykulian, Artur A, Corey, David P, Maguire, Casey A. 2017. Rescue of Hearing by Gene Delivery to Inner-Ear Hair Cells Using Exosome-Associated AAV. In Molecular therapy : the journal of the American Society of Gene Therapy, 25, 379-391. doi:10.1016/j.ymthe.2016.12.010. https://pubmed.ncbi.nlm.nih.gov/28082074/
6. Li, Xiaofen, Yu, Xiaojie, Chen, Xibing, Liu, Zhiyong, Huang, Pingbo. 2019. Localization of TMC1 and LHFPL5 in auditory hair cells in neonatal and adult mice. In FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 33, 6838-6851. doi:10.1096/fj.201802155RR. https://pubmed.ncbi.nlm.nih.gov/30808210/