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ATP10B and the risk for Parkinson’s disease

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References

  1. Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L et al (2019) Parkinson’s disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. Mov Disord 34:866–875

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Funding

This work was supported in part by the Intramural Research Programs of the National Institute of Neurological Disorders and Stroke (NINDS), the National Institute on Aging (NIA), and the National Institute of Environmental Health Sciences both part of the National Institutes of Health, Department of Health and Human Services; project numbers 1ZIA-NS003154, Z01-AG000949-02 and Z01-ES101986. In addition, this work was supported by the Department of Defense (award W81XWH-09-2-0128), and The Michael J Fox Foundation for Parkinson’s Research. Data used in the preparation of this article were obtained from the AMP PD Knowledge Platform. For up-to-date information on the study, visit https://www.amp-pd.org. AMP PD—a public-private partnership—is managed by the FNIH and funded by Celgene, GSK, the Michael J. Fox Foundation for Parkinson’s Research, the National Institute of Neurological Disorders and Stroke, Pfizer, and Verily. RR is funded by a Walker-Peltz Fellowship.

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Correspondence to Sara Bandres-Ciga.

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Real, R., Moore, A., Blauwendraat, C. et al. ATP10B and the risk for Parkinson’s disease. Acta Neuropathol 140, 401–402 (2020). https://doi.org/10.1007/s00401-020-02172-4

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  • DOI: https://doi.org/10.1007/s00401-020-02172-4

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