Reply: ATP10B variants in Parkinson’s disease—a large cohort study in Chinese mainland population
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine
Link
https://link.springer.com/content/pdf/10.1007/s00401-021-02281-8.pdf
Reference8 articles.
1. Li C, Ou R, Chen Y, Gu X, Wei Q, Cao B et al (2020) ATP10B and the risk for early-onset Parkinson’s disease. Mov Disord 35:2359–2360. https://doi.org/10.1002/mds.28285
2. Logsdon GA, Vollger MR, Eichler EE (2020) Long-read human genome sequencing and its applications. Nat Rev Genet 21:597–614. https://doi.org/10.1038/s41576-020-0236-x
3. Martin S, Smolders S, Van den Haute C, Heeman B, van Veen S, Crosiers D et al (2020) Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export. Acta Neuropathol 139:1001–1024. https://doi.org/10.1007/s00401-020-02145-7
4. Real R, Moore A, Blauwendraat C, Morris HR, Bandres-Ciga S, International Parkinson’s Disease Genomics C (2020) ATP10B and the risk for Parkinson’s disease. Acta Neuropathol 140:401–402. https://doi.org/10.1007/s00401-020-02172-4
5. Smolders S, Van Broeckhoven C (2020) Reply: ATP10B and the risk for Parkinson’s disease. Acta Neuropathol 140:403–404. https://doi.org/10.1007/s00401-020-02173-3
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