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Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.
J Mol Neurosci. 2021 Jan;71(1):142-152. doi: 10.1007/s12031-020-01635-3. Epub 2020 Jun 16.
J Mol Neurosci. 2021.
PMID: 32557143
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.
Bouhouche A, Tibar H, Kriouale Y, Jiddane M, Smaili I, Bouslam N, Benomar A, Yahyaoui M, El Fahime E.
Bouhouche A, et al. Among authors: smaili i.
Case Rep Genet. 2018 Nov 15;2018:8635698. doi: 10.1155/2018/8635698. eCollection 2018.
Case Rep Genet. 2018.
PMID: 30581635
Free PMC article.
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Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report.
Ouchkat F, Regragui W, Smaili I, Naciri Darai H, Bouslam N, Rahmani M, Melhaoui A, Arkha Y, El Fahime E, Bouhouche A.
Ouchkat F, et al. Among authors: smaili i.
BMC Med Genet. 2020 Mar 4;21(1):47. doi: 10.1186/s12881-020-0983-8.
BMC Med Genet. 2020.
PMID: 32131761
Free PMC article.
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A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia.
Smaili I, Hajjaj I, Razine R, Tibar H, Salmi A, Bouslam N, Moussa A, Regragui W, Bouhouche A.
Smaili I, et al.
Case Rep Genet. 2020 Dec 3;2020:8813344. doi: 10.1155/2020/8813344. eCollection 2020.
Case Rep Genet. 2020.
PMID: 33343949
Free PMC article.
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Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.
Smaili I, Tibar H, Rahmani M, Machkour N, Razine R, Darai HN, Bouslam N, Benomar A, Regragui W, Bouhouche A.
Smaili I, et al.
J Mol Neurosci. 2023 Jun;73(6):391-402. doi: 10.1007/s12031-023-02128-9. Epub 2023 May 31.
J Mol Neurosci. 2023.
PMID: 37256495
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