A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
- PMID: 17940179
- PMCID: PMC2117589
- DOI: 10.1136/jnnp.2007.115774
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
Conflict of interest statement
Competing interests: None.
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- Lawson V H, Graham B V, Flanigan K M. Clinical and electrophysiologic features of CMT2A with mutations in the mitofusin 2 gene. Neurology 200565197–204. - PubMed
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