1. Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease
   Cara R. Schiavon et al, 2021, Frontiers in Cell and Developmental Biology CrossRef
2. A Novel ENU-Induced Mfn2 Mutation Causes Motor Deficits in Mice without Causing Peripheral Neuropathy
   Timothy J. Hines et al, 2023, Biology CrossRef
3. Clinical and genetic diversities of Charcot‐Marie‐Tooth disease with MFN2 mutations in a large case study
   Masahiro Ando et al, 2017, Journal of the Peripheral Nervous System CrossRef
4. Hereditary neuropathies in childhood
   Pavel Seeman, 2022, Neurologie pro praxi CrossRef
5. Massively Parallel Sequencing Detected a Mutation in the MFN2 Gene Missed by Sanger Sequencing Due to a Primer Mismatch on an SNP Site
   Jana Neupauerová et al, 2016, Annals of Human Genetics CrossRef
6. Improving diagnosis of inherited peripheral neuropathies through gene panel analysis
   Petra Laššuthová et al, 2016, Orphanet Journal of Rare Diseases CrossRef
7. An integrative analysis of genotype-phenotype correlation in Charcot Marie Tooth type 2A disease with MFN2 variants: A case and systematic review
   Yuanzhu Zhang et al, 2023, Gene CrossRef
8. Mosaicism for a pathogenic MFN2 mutation causes minimal clinical features of CMT2A in the parent of a severely affected child
   Katherine Schon et al, 2017, neurogenetics CrossRef
9. Mitochondrial hyperfusion: a friend or a foe
   Rajdeep Das et al, 2020, Biochemical Society Transactions CrossRef