Cite
HARVARD Citation
Finsterer, J. et al. (n.d.). CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder. European journal of paediatric neurology. pp. 889-891. [Online].
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Finsterer, J. et al. (n.d.). CMT2 due to homozygous MFN2 variants is a multiorgan mitochondrial disorder. European journal of paediatric neurology. pp. 889-891. [Online].