1. Zhang, Fan, Wu, Zhiwei, Long, Fei, Li, Xiaorong, Lin, Changwei. 2022. The Roles of ATP13A2 Gene Mutations Leading to Abnormal Aggregation of α-Synuclein in Parkinson's Disease. In Frontiers in cellular neuroscience, 16, 927682. doi:10.3389/fncel.2022.927682. https://pubmed.ncbi.nlm.nih.gov/35875356/
2. van Veen, Sarah, Martin, Shaun, Van den Haute, Chris, Eggermont, Jan, Vangheluwe, Peter. 2020. ATP13A2 deficiency disrupts lysosomal polyamine export. In Nature, 578, 419-424. doi:10.1038/s41586-020-1968-7. https://pubmed.ncbi.nlm.nih.gov/31996848/
3. Yang, Xinglong, Xu, Yanming. 2014. Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review. In BioMed research international, 2014, 371256. doi:10.1155/2014/371256. https://pubmed.ncbi.nlm.nih.gov/25197640/
4. Dhanushkodi, Nisha R, Abul Khair, Salema B, Ardah, Mustafa T, Haque, M Emdadul. 2023. ATP13A2 Gene Silencing in Drosophila Affects Autophagic Degradation of A53T Mutant α-Synuclein. In International journal of molecular sciences, 24, . doi:10.3390/ijms24021775. https://pubmed.ncbi.nlm.nih.gov/36675288/
5. Jia, Fangzhi, Fellner, Avi, Kumar, Kishore Raj. 2022. Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing. In Genes, 13, . doi:10.3390/genes13030471. https://pubmed.ncbi.nlm.nih.gov/35328025/
6. Hayflick, Susan J, Kurian, Manju A, Hogarth, Penelope. . Neurodegeneration with brain iron accumulation. In Handbook of clinical neurology, 147, 293-305. doi:10.1016/B978-0-444-63233-3.00019-1. https://pubmed.ncbi.nlm.nih.gov/29325618/