Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency -- Bugiani et al. 42 (5): e28 Data Supplement

Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
M Bugiani, V Tiranti, L Farina, G Uziel, and M Zeviani

There is an error in the nomenclature of the two mutations reported in this article. In both the main text and Table 1 the nomenclature should read as follows:

503C->G should read 452C->G
The corresponding aminoacid should read S151X instead of H152X.
and
1081T->C should read 1030T->C
The corresponding aminoacid reads correctly (S344P).