Skip to main content
Log in

ATP10B variants in Parkinson’s disease: a large cohort study in Chinese mainland population

  • Correspondence
  • Published:
Acta Neuropathologica Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

References

  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

    Article  CAS  PubMed  Google Scholar 

  2. 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

    Article  PubMed  PubMed Central  Google Scholar 

  3. 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

    Article  PubMed  Google Scholar 

  4. 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

    Article  PubMed  Google Scholar 

  5. Smolders S, Van Broeckhoven C (2020) Reply: segregation of ATP10B variants in families with autosomal recessive Parkinsonism. Acta Neuropathol 140:787–789. https://doi.org/10.1007/s00401-020-02220-z

    Article  CAS  PubMed  Google Scholar 

  6. Tesson C, Lohmann E, Devos D, Bertrand H, Lesage S, Brice A (2020) Segregation of ATP10B variants in families with autosomal recessive Parkinsonism. Acta Neuropathol 140:783–785. https://doi.org/10.1007/s00401-020-02219-6

    Article  CAS  PubMed  Google Scholar 

  7. Zhao Y, Qin L, Pan H, Liu Z, Jiang L, He Y et al (2020) The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population. Brain 143:2220–2234. https://doi.org/10.1093/brain/awaa167

    Article  PubMed  Google Scholar 

Download references

Funding

This study was supported by the National Natural Science Foundation of China (Grant No. 82001359 and No. U20A20355), the National Key Research and Development Program of China (Grant No. 2016YFC1306000) and Hunan Innovative Province Construction Project (Grant No. 2019SK2335).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhenhua Liu.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (PDF 2833 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Zhao, Y., Pan, H., Wang, Y. et al. ATP10B variants in Parkinson’s disease: a large cohort study in Chinese mainland population. Acta Neuropathol 141, 805–806 (2021). https://doi.org/10.1007/s00401-021-02280-9

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00401-021-02280-9

Navigation