1. Wang, Pin, Wang, Lei, Sha, Jie, Mao, Jian-Hua, Zou, Xiaoping. 2017. Expression and Transcriptional Regulation of Human ATP6V1A Gene in Gastric Cancers. In Scientific reports, 7, 3015. doi:10.1038/s41598-017-03021-3. https://pubmed.ncbi.nlm.nih.gov/28592880/
2. Conte, Federica, Sam, Juda-El, Lefeber, Dirk J, Passier, Robert. 2023. Metabolic Cardiomyopathies and Cardiac Defects in Inherited Disorders of Carbohydrate Metabolism: A Systematic Review. In International journal of molecular sciences, 24, . doi:10.3390/ijms24108632. https://pubmed.ncbi.nlm.nih.gov/37239976/
3. Shariq, Mohd, Khan, Mohammad Firoz, Raj, Reshmi, Ahsan, Nuzhat, Kumar, Pramod. 2024. PRKAA2, MTOR, and TFEB in the regulation of lysosomal damage response and autophagy. In Journal of molecular medicine (Berlin, Germany), 102, 287-311. doi:10.1007/s00109-023-02411-7. https://pubmed.ncbi.nlm.nih.gov/38183492/
4. Kadwa, Razia A. 2020. Novel Mutation in ATP6V1A Gene with Infantile Spasms in an Indian Boy. In Neuropediatrics, 51, 292-294. doi:10.1055/s-0040-1701657. https://pubmed.ncbi.nlm.nih.gov/32045939/
5. Xiaoquan, Chen, Yuting, Lou, Pu, Miao, Mengmeng, Liang, Jianhua, Feng. 2023. A heterozygous pathogenic variant in the ATP6V1A gene triggering epilepsy in a large Chinese pedigree. In Clinical neurology and neurosurgery, 233, 107956. doi:10.1016/j.clineuro.2023.107956. https://pubmed.ncbi.nlm.nih.gov/37729800/
6. Fassio, Anna, Esposito, Alessandro, Kato, Mitsuhiro, Benfenati, Fabio, Guerrini, Renzo. . De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy. In Brain : a journal of neurology, 141, 1703-1718. doi:10.1093/brain/awy092. https://pubmed.ncbi.nlm.nih.gov/29668857/
7. Zhou, Zhike, Bai, Jun, Zhong, Shanshan, Zhao, Chuansheng, Zhao, Mei. 2021. Downregulation of ATP6V1A Involved in Alzheimer's Disease via Synaptic Vesicle Cycle, Phagosome, and Oxidative Phosphorylation. In Oxidative medicine and cellular longevity, 2021, 5555634. doi:10.1155/2021/5555634. https://pubmed.ncbi.nlm.nih.gov/33981384/
智鼠故事 
