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HARVARD Citation
Iapadre, G. et al. (n.d.). A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype. European journal of paediatric neurology. pp. 563-567. [Online].
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Iapadre, G. et al. (n.d.). A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype. European journal of paediatric neurology. pp. 563-567. [Online].