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Phenotypic spectrum of MFN2 mutations in the Spanish population
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    Does c.892G>A missense point mutation (Gly298Arg) in MFN2 cause CMT-2A?

    It was with great interest that I read Casasnovas et al article "Phenotypic Spectrum of MFN2 Mutations in the Spanish Population". The authors mention the Gly298Arg mutation in one of their families, with 2 affected individuals, and state that this has previously been described. They refer to Lawson's 2005 article (Ref#10, Lawson VH, Graham BV, Flanigan KM. Clinical and electrophysiologic features of CMT2A with mutation...

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    Conflict of Interest:
    None declared.