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The p.Gly2019Ser is a common LRRK2 pathogenic variant among Egyptians with familial and sporadic Parkinson's disease.
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- NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00826-8
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- Article
Health inequity in genomic personalized medicine in underrepresented populations: a look at the current evidence.
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- Functional & Integrative Genomics, 2023, v. 23, n. 1, p. 1, doi. 10.1007/s10142-023-00979-4
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- Article