Publications by authors named "Wafaa Regragui"

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Novel Variants in Two Moroccan Families with Wolfram Syndrome.
Ahmed Bouhouche, Sara Sefiani, Hicham Charoute, Tibar Houyam, Naima Bouslam, Wafaa Regragui

Genet Test Mol Biomarkers· June 2024

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Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report.
Fatima Ouchkat, Wafaa Regragui, Imane Smaili, Hajar Naciri Darai, Naima Bouslam

BMC Med Genet· March 2020

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Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.
Ahmed Bouhouche, Christelle Tesson, Wafaa Regragui, Mounia Rahmani, Valérie Drouet

Front Neurol· October 2017

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A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.
Rafiqua Ben El Haj, Wafaa Regragui, Rachid Tazi-Ahnini, Asmae Skalli, Naima Bouslam

Biomed Res Int· March 2017

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Clinical and genetic data of Huntington disease in Moroccan patients.
Ahmed Bouhouche, Wafaa Regragui, Hind Lamghari, Khadija Khaldi, Nazha Birouk

Afr Health Sci· December 2015

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