Rare Variants Cause Charcot‐Marie‐Tooth Disease in Malian Families
This study reports rare variants in these CMT genes for the first time in SSA populations, expanding the global epidemiological, clinical, and genetic spectrum of these diseases.
Authors
- Abdoulaye Yalcouyé (ORCID: https://orcid.org/0000-0003-4279-7380)
- Dramane Coulibaly (ORCID: https://orcid.org/0000-0001-8280-1685)
- Vorasuk Shotelersuk (ORCID: https://orcid.org/0000-0002-1856-0589)
- Patra Yeetong (ORCID: https://orcid.org/0000-0001-8860-7904)
- Guida Landouré (ORCID: https://orcid.org/0000-0002-5921-7832)
- Alassane Baneye Maīga (ORCID: https://orcid.org/0000-0002-7296-7785)
- Boubacar Maïga (ORCID: https://orcid.org/0000-0001-7935-3674)
- Lassana Cissé (ORCID: https://orcid.org/0000-0001-6574-0956)
- Kenneth H. Fischbeck (ORCID: https://orcid.org/0000-0002-8316-6895)
- Hamidou Oumar Bâ
- Salia Bamba (ORCID: https://orcid.org/0000-0002-1680-5183)
- Abdoulaye Taméga
- Salimata Diallo
- Salimata Diarra (ORCID: https://orcid.org/0000-0003-2160-9942)
- Seybou Hassane Diallo
- Kékouta Dembélé
- Cheick O. Guinto
Institutions
- Thai Red Cross Society (TH)
- Johns Hopkins University (US)
- Chulalongkorn University (TH)
- Centre Hospitalier de Luxembourg (LU)
- King Chulalongkorn Memorial Hospital (TH)
- University of Bamako (ML)
- National Institute of Neurological Disorders and Stroke (US)
- Université des Sciences, des Techniques et des Technologies de Bamako (ML)
- Mali-Folkecenter (ML)
Publication Details
- Journal
- Brain and Behavior
- Published
- 2025-05-01
- DOI
- https://doi.org/10.1002/brb3.70496
- Citations
- 1
- Primary Topic
- Hereditary Neurological Disorders
- Type
- article
- Field-Weighted Citation Impact
- 0.91
Funders
- National Institute of Neurological Disorders and Stroke