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MFN2 gene

Discuss publications and research concerning the MFN2 gene.

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Related literature

Late-onset hereditary sensory and autonomic neuropathy expands the phenotypic spectrum of MFN2-related diseases.
MFN2
Mitochondrial hyperfusion causes neuropathy in a fly model of CMT2A.
MFN2
Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression.
MFN2
A novel p.Val244Leu mutation in MFN2 leads to Charcot-Marie-Tooth disease type 2.
MFN2
[Pathology of Charcot-Marie-Tooth Disease].
MFN2
Mutational mechanisms in MFN2-related neuropathy: compound heterozygosity for recessive and semidominant mutations.
MFN2
MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.
MFN2
Acute optic neuropathy associated with a novel MFN2 mutation.
MFN2
Emery-Dreifuss muscular dystrophy type 2 associated (?) with mild peripheral polyneuropathy.
MFN2
Mitofusin 2 expression dominates over mitofusin 1 exclusively in mouse dorsal root ganglia - a possible explanation for peripheral nervous system involvement in Charcot-Marie-Tooth 2A.
MFN2

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