Associated Papers
SURF1 deficiency: a multi-centre natural history study.
Wedatilake Y et al.
Orphanet Journal of Rare Diseases, 2013
Mutations in the SURF1 gene associated with Leigh syndrome and cytochrome C oxidase deficiency.
Péquignot MO et al.
Human Mutation, 2001
Nuclear gene defects in mitochondrial disorders.
Zeviani M et al.
Italian Journal of Neurological Sciences, 1999
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