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The Impact of Recent Demography on Functional Genetic Variation in North African Human Groups.
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- Molecular Biology & Evolution, 2024, v. 41, n. 1, p. 1, doi. 10.1093/molbev/msad283
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- Article
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
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- Human Molecular Genetics, 2010, v. 19, n. 10, p. 1998
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- Article
Purification and characterization of a platelet aggregation inhibitor and anticoagulant Cc 5_NTase, CD 73-like, from Cerastes cerastes venom.
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- Journal of Biochemical & Molecular Toxicology, 2017, v. 31, n. 5, p. N/A, doi. 10.1002/jbt.21885
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- Article
Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases.
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- Journal of Neurology, 2016, v. 263, n. 7, p. 1314, doi. 10.1007/s00415-016-8112-5
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Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
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- BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0180-3
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- Article
Whole mitogenomes reveal that NW Africa has acted both as a source and a destination for multiple human movements.
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- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-37549-4
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- Article
Isolation of atypical wheat-associated xanthomonads in Algeria.
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- Phytopathologia Mediterranea, 2019, v. 58, n. 3, p. 497, doi. 10.14601/Phyto-10855
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Ankylosing spondylitis: analysis of gene-gene interactions between IL-12β, JAK2, and STAT3 in Han Chinese and Algerian cohorts.
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- Central European Journal of Immunology, 2019, v. 44, n. 1, p. 65, doi. 10.5114/ceji.2019.84019
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- Article
Understanding the genomic heterogeneity of North African Imazighen: from broad to microgeographical perspectives.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-60568-8
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- Article