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BMC Medical Genetics|March 6, 2020
Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case reportFatima Ouchkat, Wafaa Regragui, Imane Smaili, et al.
Genetic Testing and Molecular Biomarkers|May 9, 2024
Novel WFS1 Variants in Two Moroccan Families with Wolfram SyndromeAhmed Bouhouche, Sara Sefiani, Hicham Charoute, et al.
Brain : a Journal of Neurology|January 26, 2006
Autosomal recessive spastic paraplegia (SPG30) with mild ataxia and sensory neuropathy maps to chromosome 2q37.3Stephan Klebe, Hamid Azzedine, Alexandra Durr, et al.
Annals of Neurology|March 24, 2005
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)Naima Bouslam, Ali Benomar, Hamid Azzedine, et al.
Journal of the Neurological Sciences|June 1, 2002
Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan familiesAli Benomar, Mohammed Yahyaoui, Farid Meggouh, et al.
BMC Medical Genetics|March 23, 2012
An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3Ahmed Bouhouche, Ali Benomar, Leila Errguig, et al.
Parkinson'S Disease|May 4, 2017
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's DiseaseAhmed Bouhouche, Houyam Tibar, Rafiqua Ben El Haj, et al.
Archives of Neurology|August 18, 2004
Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14Giovanni Stevanin, Valérie Hahn, Ebba Lohmann, et al.
Journal of Medical Genetics|December 10, 2013
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunctionTalya Dor, Yuval Cinnamon, Laure Raymond, et al.
Frontiers in Neurology|November 23, 2017
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene PanelAhmed Bouhouche, Christelle Tesson, Wafaa Regragui, et al.
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