Disease: Charcot-Marie-Tooth disease- Type 2A
- A case report of concurrent occurrence of two inherited axonopathies within a family: the benefit of whole-exome sequencing
- A human mitofusin 2 mutation can cause mitophagic cardiomyopathy
- A Novel ENU-Induced <em>Mfn2</em> Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy
- A SARM1-mitochondrial feedback loop drives neuropathogenesis in a Charcot-Marie-Tooth disease type 2A rat model
- Aberrant Mitochondrial Dynamics and Exacerbated Response to Neuroinflammation in a Novel Mouse Model of CMT2A
- An integrative analysis of genotype-phenotype correlation in Charcot Marie Tooth type 2A disease with MFN2 variants: A case and systematic review
- Analysis of a pedigree with distal hereditary motor neuropathy type 2A caused by mutation in HSPB8 gene
- Case report: Asp194Ala variant in MFN2 is associated with ALS-FTD in an Italian family
- Characterization of a novel variant in the HR1 domain of <em>MFN2</em> in a patient with ataxia, optic atrophy and sensorineural hearing loss
- Charcot-Marie-tooth disease type 2A: An update on pathogenesis and therapeutic perspectives
- Charcot-Marie-Tooth type 2A in vivo models: Current updates
- Clinical and genetic features of a cohort of patients with MFN2-related neuropathy
- Corrigendum to "Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2" [Stem Cell Res. 36C (2019) 101411]
- Corrigendum to "Generation of induced pluripotent stem cell line, ZJUCHi002-A, from Charcot-Marie-Tooth disease type 2A (CMT2A) patient with a mutation of c.752C>T in MFN2" [Stem Cell Res. 36C (2019) 101411]
- Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A
- Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A
- Homozygous Mutations in <em>GDAP1</em> and <em>MFN2</em> Genes Resulted in Autosomal Recessive Forms of Charcot-Marie-Tooth Disease in Consanguineous Pakistani Families
- MFN1 augmentation prevents retinal degeneration in a Charcot-Marie-Tooth type 2A mouse model
- Microrchidia CW-Type Zinc Finger 2, a Chromatin Modifier in a Spectrum of Peripheral Neuropathies
- Mitochondria Clumping vs. Mitochondria Fusion in CMT2A Diseases
- Mitochondrial Dysfunction and Pharmacodynamics of Mitofusin Activation in Murine Charcot-Marie-Tooth Disease Type 2A
- Mitochondrial Phenotypes in Genetically Diverse Neurodegenerative Diseases and Their Response to Mitofusin Activation
- Mitofusin 2 mutation drives cell proliferation in Charcot-Marie-Tooth 2A fibroblasts
- Mitofusin 2: The missing link between mtDNA maintenance defects and neurotransmitter disorders
- Predicting Mitochondrial Dynamic Behavior in Genetically Defined Neurodegenerative Diseases
- Tetrahydroquinoline-Capped Histone Deacetylase 6 Inhibitor SW-101 Ameliorates Pathological Phenotypes in a Charcot-Marie-Tooth Type 2A Mouse Model
- The Genotype and Phenotype Features in a Large Chinese MFN2 Mutation Cohort
- The Pathological Features of Common Hereditary Mitochondrial Dynamics Neuropathy
- Torin1 restores proliferation rate in Charcot-Marie-Tooth disease type 2A cells harbouring MFN2 (mitofusin 2) mutation
- Variants of uncertain significance in the era of next-generation sequencing