Associated Papers
Clinical Diagnosis and Treatment of Leigh Syndrome Based on SURF1: Genotype and Phenotype.
Lee IC et al.
Antioxidants (basel, Switzerland), 2021
SURF1 deficiency: a multi-centre natural history study.
Wedatilake Y et al.
Orphanet Journal of Rare Diseases, 2013
SURF1-associated Leigh syndrome: a case series and novel mutations.
Lee IC et al.
Human Mutation, 2012
Novel SURF1 mutation in a child with subacute encephalopathy and without the radiological features of Leigh Syndrome.
Salviati L et al.
American Journal of Medical Genetics. Part A, 2004
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