Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12031-023-02128-9.pdf
Reference44 articles.
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3. Bandrés-Ciga S, Diez-Fairen M, Kim JJ, Singleton AB (2020) Genetics of Parkinson’s disease: an introspection of its journey towards precision medicine. Neurobiol Dis 137:104782
4. Bayne AN, Trempe JF (2019) Mechanisms of PINK1, ubiquitin and Parkin interactions in mitochondrial quality control and beyond. Cell Mol Life Sci 76:4589–4611
5. Ben El Haj R, Salmi A, Regragui W, Moussa A, Bouslam N, Tibar H, Benomar A, Yahyaoui M, Bouhouche A (2017) Evidence for prehistoric origins of the G2019S mutation in the North African Berber population. PLoS ONE 12:e0181335
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