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Case Reports
. 2023 Sep;38(9):1756-1757.
doi: 10.1002/mds.29533. Epub 2023 Jul 11.

Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease

Christelle Tesson  1 , Mohamed Sofiane Bouchetara  2 , Mélanie Ferrien  1 , Suzanne Lesage  1 , Alexis Brice  1   3
Affiliations
Case Reports

Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease

Christelle Tesson et al. Mov Disord. 2023 Sep.
No abstract available

Keywords: DAGLB; Parkinson disease; autosomal recessive inheritance; early-onset.

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References

    1. Liu Z, Yang N, Dong J, et al. Deficiency in endocannabinoid synthase DAGLB contributes to early onset parkinsonism and murine nigral dopaminergic neuron dysfunction. Nat Commun 2022;13:3490. https://doi.org/10.1038/s41467-022-31168-9
    1. Rodrigues CHM, Pires DEV, Ascher DB. DynaMut2: assessing changes in stability and flexibility upon single and multiple point missense mutations. Protein Sci 2021;30(1):60-69. https://doi.org/10.1002/pro.3942
    1. Lücking CB, Dürr A, Bonifati V, et al. Association between early-onset Parkinson's disease and mutations in the Parkin gene. N Engl J Med 2000;342(21):1560-1567. https://doi.org/10.1056/NEJM200005253422103
    1. Ibáñez P, Lesage S, Lohmann E, et al. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain 2006;129(Pt 3):686-694. https://doi.org/10.1093/brain/awl005

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