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Annals of Neurology|January 27, 2006
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2Stephan Züchner, Peter De Jonghe, Albena Jordanova, et al.Journal of Neurology, Neurosurgery, and Psychiatry|May 15, 2017
Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth diseaseAlejandro Horga, Matilde Laurà, Zane Jaunmuktane, et al.Neurology|December 3, 2021
Phase 2 Trial of Rituximab in Acetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis: The BeatMG StudyRichard J Nowak, Christopher S Coffey, Jonathan M Goldstein, et al.Cell Reports|August 11, 2015
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex NeuropathyClaudia Gonzaga-Jauregui, Tamar Harel, Tomasz Gambin, et al.Brain : a Journal of Neurology|September 28, 2023
Genetic landscape of congenital insensitivity to pain and hereditary sensory and autonomic neuropathiesAnnette Lischka, Katja Eggermann, Christopher J Record, et al.Pageof 5