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Article

Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.

Neurology - 9 Aug 2005

Zhu D, Kennerson M L, Walizada G, Züchner S, Vance J M, Nicholson G A

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Source

Identifiers

PMID: 16087932
DOI: 10.1212/01.wnl.0000171345.62270.29

Genes

MFN2

Provenance

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Related research

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Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations.PMID 16087932Read ↗

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Charcot–Marie–Tooth disease and related disorders: an evolving landscapeSemantic proximity Read ↗

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An integrative analysis of genotype-phenotype correlation in Charcot Marie Tooth type 2A disease with MFN2 variants: A case and systematic review.Semantic proximity Read ↗

Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypes.Semantic proximity Read ↗

CMT with pyramidal features. Charcot-Marie-Tooth.Semantic proximity Read ↗

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

The various Charcot-Marie-Tooth diseases.Semantic proximity Read ↗

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

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

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