Rare Variants Cause Charcot‐Marie‐Tooth Disease in Malian Families

Rare Variants Cause Charcot‐Marie‐Tooth Disease in Malian Families

ABSTRACT Introduction/Aims Charcot‐Marie‐Tooth disease (CMT), the most common inherited peripheral neuropathy, is clinically and genetically heterogeneous with over 100 genes identified to date. Recently, next‐generation sequencing (NGS) has enabled molecular diagnosis in previously unidentified CMT...

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Main Authors: Abdoulaye Yalcouyé, Lassana Cissé, Salimata Diarra, Seybou H. Diallo, Salia Bamba, Patra Yeetong, Boubacar Maiga, Kékouta Dembélé, Dramane Coulibaly, Salimata Diallo, Abdoulaye Taméga, Alassane Baneye Maiga, Hamidou O. Ba, Vorasuk Shotelersuk, Kenneth H. Fischbeck, Cheick O. Guinto, Guida Landouré
Format: Article
Language:English
Published: Wiley 2025-05-01
Series:Brain and Behavior
Subjects:
Africa
BAG3
BSCL2
Charcot‐Marie‐Tooth disease
Mali
PEX10
Online Access:https://doi.org/10.1002/brb3.70496
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https://doi.org/10.1002/brb3.70496

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