MFN2, a new gene responsible for mitochondrial DNA depletion

Large Kindred Evaluation of Mitofusin 2 Novel Mutation, Extremes of Neurologic Presentations, and Preserved Nerve Mitochondria

(2011) Christopher J. Klein   ARCHIVES OF NEUROLOGY

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype

(2011) C. Rouzier et al.   BRAIN

Defects in mitochondrial DNA replication and human disease

(2011) William C. Copeland   CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY

Characterizing the phenotypic manifestations of MFN2 R104W mutation in Charcot–Marie–Tooth type 2

(2011) Adriana Borges Genari et al.   NEUROMUSCULAR DISORDERS

Mitochondrial Fusion Is Required for mtDNA Stability in Skeletal Muscle and Tolerance of mtDNA Mutations

(2010) Hsiuchen Chen et al.   CELL

SEVERE CMT TYPE 2 WITH FATAL ENCEPHALOPATHY ASSOCIATED WITH A NOVEL MFN2 SPLICING MUTATION

(2010) F. Boaretto et al.   NEUROLOGY

Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations

(2008) Knut Brockmann et al.   JOURNAL OF NEUROLOGY

Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction

(2008) R. D. Bo et al.   NEUROLOGY