1. Nascimento, Andres, Bruels, Christine C, Donkervoort, Sandra, Kang, Peter B, Natera-de Benito, Daniel. 2023. Variants in DTNA cause a mild, dominantly inherited muscular dystrophy. In Acta neuropathologica, 145, 479-496. doi:10.1007/s00401-023-02551-7. https://pubmed.ncbi.nlm.nih.gov/36799992/
2. Lopez-Escamez, Jose A, Liu, Ying. 2023. Epidemiology and genetics of Meniere's disease. In Current opinion in neurology, 37, 88-94. doi:10.1097/WCO.0000000000001227. https://pubmed.ncbi.nlm.nih.gov/37865853/
3. Hu, Zhi-Gao, Zhang, Shun, Chen, Yu-Bing, Gao, Ge, He, Song-Qing. 2020. DTNA promotes HBV-induced hepatocellular carcinoma progression by activating STAT3 and regulating TGFβ1 and P53 signaling. In Life sciences, 258, 118029. doi:10.1016/j.lfs.2020.118029. https://pubmed.ncbi.nlm.nih.gov/32619495/
4. Wu, Yukang, Guo, Xudong, Han, Tong, Wan, Xiaoping, Kang, Jiuhong. 2022. Cmarr/miR-540-3p axis promotes cardiomyocyte maturation transition by orchestrating Dtna expression. In Molecular therapy. Nucleic acids, 29, 481-497. doi:10.1016/j.omtn.2022.07.022. https://pubmed.ncbi.nlm.nih.gov/36035750/
5. Lesurf, Robert, Said, Abdelrahman, Akinrinade, Oyediran, Scherer, Stephen W, Mital, Seema. 2022. Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathy. In NPJ genomic medicine, 7, 18. doi:10.1038/s41525-022-00288-y. https://pubmed.ncbi.nlm.nih.gov/35288587/
6. Yao, Di, Li, Rong, Hao, Jiahuan, Liu, Xinghua, Wang, Minghuan. 2023. Melatonin alleviates depression-like behaviors and cognitive dysfunction in mice by regulating the circadian rhythm of AQP4 polarization. In Translational psychiatry, 13, 310. doi:10.1038/s41398-023-02614-z. https://pubmed.ncbi.nlm.nih.gov/37802998/
7. Malakootian, Mahshid, Jalilian, Masoumeh, Kalayinia, Samira, Heidarali, Mona, Haghjoo, Majid. 2022. Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation. In BMC cardiovascular disorders, 22, 37. doi:10.1186/s12872-022-02485-0. https://pubmed.ncbi.nlm.nih.gov/35148685/