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Comment
. 2023 Dec 1;146(12):e120-e124.
doi: 10.1093/brain/awad247.

PTPA variants and the risk for Parkinson's disease in diverse ancestry populations

Miriam Ostrožovičová  1   2 , Yasser Mecheri  3 , Bashayer R Al-Mubarak  4 , Nada Al-Tassan  4 , Mary B Makarious  5   6 , Maria Teresa Periñan  7   8 , Sara Bandres-Ciga  9
Affiliations
Comment

PTPA variants and the risk for Parkinson's disease in diverse ancestry populations

Miriam Ostrožovičová et al. Brain. .
No abstract available

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Conflict of interest statement

The authors report no competing interests.

Comment on

  • PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability.
    Fevga C, Tesson C, Carreras Mascaro A, Courtin T, van Coller R, Sakka S, Ferraro F, Farhat N, Bardien S, Damak M, Carr J, Ferrien M, Boumeester V, Hundscheid J, Grillenzoni N, Kessissoglou IA, Kuipers DJS, Quadri M; French and Mediterranean Parkinson disease Genetics Study Group; International Parkinsonism Genetics Network; Corvol JC, Mhiri C, Hassan BA, Breedveld GJ, Lesage S, Mandemakers W, Brice A, Bonifati V. Fevga C, et al. Brain. 2023 Apr 19;146(4):1496-1510. doi: 10.1093/brain/awac326. Brain. 2023. PMID: 36073231 Free PMC article.

References

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    1. Sandal P, Jong CJ, Merrill RA, Song J, Strack S. Protein phosphatase 2A—structure, function and role in neurodevelopmental disorders. J Cell Sci. 2021;134:jcs248187. - PMC - PubMed
    1. Yemni EA, Monies D, Alkhairallah T, et al. Integrated analysis of whole exome sequencing and copy number evaluation in Parkinson’s disease. Sci Rep. 2019;9:3344. - PMC - PubMed
    1. Wang K, Li M, Hakonarson H. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res. 2010;38:e164. - PMC - PubMed
    1. Chang CC, Chow CC, Tellier LC, Vattikuti S, Purcell SM, Lee JJ. Second-generation PLINK: rising to the challenge of larger and richer datasets. Gigascience. 2015;4:7. - PMC - PubMed

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