1. Li, Xiaolu, Yang, Ye, Xu, Senming, Chen, Jianmin, Xu, Jianwen. 2023. Screening biomarkers for spinal cord injury using weighted gene co-expression network analysis and machine learning. In Neural regeneration research, 19, 2723-2734. doi:10.4103/1673-5374.391306. https://pubmed.ncbi.nlm.nih.gov/38595290/
2. Pedemonte, Nicoletta, Galietta, Luis J V. . Structure and function of TMEM16 proteins (anoctamins). In Physiological reviews, 94, 419-59. doi:10.1152/physrev.00039.2011. https://pubmed.ncbi.nlm.nih.gov/24692353/
3. Milovanović, Andona, Westenberger, Ana, Stanković, Iva, Kostić, Vladimir S, Dragašević-Mišković, Natasa. 2024. ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series. In Movement disorders : official journal of the Movement Disorder Society, 39, 887-892. doi:10.1002/mds.29729. https://pubmed.ncbi.nlm.nih.gov/38469933/
4. Massey, Sean, Guo, Yiran, Riley, Lisa G, Cooper, Sandra, Christodoulou, John. 2023. Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar Ataxia. In Neurology. Genetics, 9, e200051. doi:10.1212/NXG.0000000000200051. https://pubmed.ncbi.nlm.nih.gov/36698452/
5. Nanetti, Lorenzo, Sarto, Elisa, Castaldo, Anna, Mariotti, Caterina, Taroni, Franco. 2018. ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype. In Journal of neurology, 266, 378-385. doi:10.1007/s00415-018-9141-z. https://pubmed.ncbi.nlm.nih.gov/30515630/
6. Wanitchakool, Podchanart, Ousingsawat, Jiraporn, Sirianant, Lalida, Schreiber, Rainer, Kunzelmann, Karl. 2016. Cellular defects by deletion of ANO10 are due to deregulated local calcium signaling. In Cellular signalling, 30, 41-49. doi:10.1016/j.cellsig.2016.11.006. https://pubmed.ncbi.nlm.nih.gov/27838374/
7. Balreira, Andrea, Boczonadi, Veronika, Barca, Emanuele, Quinzii, Catarina M, Horvath, Rita. 2014. ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency. In Journal of neurology, 261, 2192-8. doi:10.1007/s00415-014-7476-7. https://pubmed.ncbi.nlm.nih.gov/25182700/
8. Koenig, Michel, Tranchant, Christine, Anheim, Mathieu. . Autosomal recessive cerebellar ataxia 3 due to homozygote c.132dupA mutation within the ANO10 gene--reply. In JAMA neurology, 72, 239-40. doi:10.1001/jamaneurol.2014.3921. https://pubmed.ncbi.nlm.nih.gov/25664551/
智鼠故事 
