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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
1 clinical trial registered, 1 recruiting. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
10 publications have been identified in PubMed for parkinsonism due to ATP13A2 deficiency. Research spans Basic Science / Preclinical (78%), Review / Meta-Analysis (11%), and Case Report / Case Series (11%).
Fujii T (2026). [PMID: 41751935](https://pubmed.ncbi.nlm.nih.gov/41751935/). *International journal of molecular sciences*. [Review / Meta-Analysis]
Murakami T (2026). [PMID: 41520027](https://pubmed.ncbi.nlm.nih.gov/41520027/). *Scientific reports*. [Basic Science / Preclinical]
Zou Z (2026). [PMID: 41843675](https://pubmed.ncbi.nlm.nih.gov/41843675/). *Proceedings of the National Academy of Sciences of the United States of America*. [Basic Science / Preclinical]
Tsunemi T (2025). [PMID: 39936955](https://pubmed.ncbi.nlm.nih.gov/39936955/). *Cells*. [Basic Science / Preclinical]
Samaddar M (2025). [PMID: 40848257](https://pubmed.ncbi.nlm.nih.gov/40848257/). *Cell reports*. [Basic Science / Preclinical]
Data assembled from 4 of 12 sources · Last updated Sep 20, 2026, 8:43 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Wang SS (2025). [PMID: 39227736](https://pubmed.ncbi.nlm.nih.gov/39227736/). *Acta pharmacologica Sinica*. [Basic Science / Preclinical]
Ti X (2025). [PMID: 40345588](https://pubmed.ncbi.nlm.nih.gov/40345588/). *The Journal of biological chemistry*. [Basic Science / Preclinical]
Colijn MA (2024). [PMID: 39023817](https://pubmed.ncbi.nlm.nih.gov/39023817/). *Neurogenetics*. [Case Report / Case Series]
Sikora J (2024). [PMID: 39090150](https://pubmed.ncbi.nlm.nih.gov/39090150/). *NPJ Parkinson's disease*. [Basic Science / Preclinical]