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Article

Charcot-Marie-Tooth Disease Associated With a Novel Mutation in MFN2 Presenting With Subacute Vision Loss.

Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society - 1 Mar 2022

Li Yafeng, Aleman Tomas S, Quinn Colin C, Xia Tian, Miller Charles G, Kim Benjamin J, Tamhankar Madhura A

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PMID: 34924536
DOI: 10.1097/WNO.0000000000001404

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Related research

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Charcot-Marie-Tooth Disease Associated With a Novel Mutation in MFN2 Presenting With Subacute Vision Loss.PMID 34924536Read ↗

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Clinical and genetic features of a cohort of patients with MFN2-related neuropathy.Semantic proximity Read ↗

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A cohort study of MFN2 mutations and phenotypic spectrums in Charcot-Marie-Tooth disease 2A patients.Semantic proximity Read ↗

Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot-Marie-Tooth type 2.Semantic proximity Read ↗

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