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Updated: Jun 26, 2025

Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome

Ahmed Bouhouche1,2, Sara Sefiani2, Hicham Charoute3

  • 1Research Team in Neurology and Neurogenetics, Center of Genomics of Human Pathologies, Medical School and Pharmacy, University Mohammed V in Rabat, Rabat, Morocco.

Genetic Testing and Molecular Biomarkers
|May 9, 2024
PubMed

Keywords:
MoroccansWFS1Wolfram syndromenovel variantswhole-exome sequencing

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