Late-onset Leigh syndrome in a patient with mitochondrial complex I NDUFS8 mutations
Vincent Procaccio1, Douglas C Wallace
1Center for Molecular and Mitochondrial Medicine and Genetics (MAMMAG), University of California, Irvine 92697-3940, USA. vproca@uci.edu
Abstract:
Analysis of the complex I NDUFS8 gene from Leigh syndrome patients with isolated complex I deficiency revealed that one patient with late-onset disease and partial complex I defect was a compound heterozygote for two novel mutations in NDUFS8 gene. Western blot analysis revealed a deficiency in the NDUFS8 polypeptide, but also reductions in other nuclear subunits of complex I, suggesting that this subunit is essential for either the assembly or stability of complex I.
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