1. Xue, Yuanyuan, Hu, Xinde, Wang, Daqi, Zuo, Erwei, Shu, Yilai. 2021. Gene editing in a Myo6 semi-dominant mouse model rescues auditory function. In Molecular therapy : the journal of the American Society of Gene Therapy, 30, 105-118. doi:10.1016/j.ymthe.2021.06.015. https://pubmed.ncbi.nlm.nih.gov/34174443/
2. Aldè, Mirko, Cantarella, Giovanna, Zanetti, Diego, Simon, Francois, Maniaci, Antonino. 2023. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review. In Biomedicines, 11, . doi:10.3390/biomedicines11061616. https://pubmed.ncbi.nlm.nih.gov/37371710/
3. Del Castillo, Ignacio, Morín, Matías, Domínguez-Ruiz, María, Moreno-Pelayo, Miguel A. 2022. Genetic etiology of non-syndromic hearing loss in Europe. In Human genetics, 141, 683-696. doi:10.1007/s00439-021-02425-6. https://pubmed.ncbi.nlm.nih.gov/35044523/
4. Carlson, Ryan J, Walsh, Tom, Mandell, Jessica B, Rubinstein, Jay, King, Mary-Claire. . Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes. In JAMA otolaryngology-- head & neck surgery, 149, 212-222. doi:10.1001/jamaoto.2022.4463. https://pubmed.ncbi.nlm.nih.gov/36633841/
5. Zheng, Shengfeng, Hong, Zhe, Tan, Yao, Lin, Guowen, Ye, Dingwei. 2024. MYO6 contributes to tumor progression and enzalutamide resistance in castration-resistant prostate cancer by activating the focal adhesion signaling pathway. In Cell communication and signaling : CCS, 22, 517. doi:10.1186/s12964-024-01897-z. https://pubmed.ncbi.nlm.nih.gov/39449086/
6. Boucher, Sophie, Tai, Fabienne Wong Jun, Delmaghani, Sedigheh, Bonnet, Crystel, Petit, Christine. 2020. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. In Proceedings of the National Academy of Sciences of the United States of America, 117, 31278-31289. doi:10.1073/pnas.2010782117. https://pubmed.ncbi.nlm.nih.gov/33229591/
智鼠故事 
