CMT2A Harboring Mitofusin 2 Mutation with Optic Nerve Atrophy and Normal Visual Acuity
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Reference17 articles.
1. Genetic and clinical aspects of Charcot-Marie-Tooth's disease
2. Annals of Neurology
3. Charcot-Marie-Tooth neuropathy type 2A: novel mutations in the mitofusin 2 gene (MFN2)
4. Autosomal recessiveMFN2-related Charcot-Marie-Tooth disease with diaphragmatic weakness: Case report and literature review
5. MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives
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