M. E. Vázquez-Memije

Comparative biochemical studies of ATPases in cells from patients with the T8993G or T8993C mitochondrial DNA mutations

S. Dimauro, F. Santorelli, D. Devivo, 1998, Journal of Inherited Metabolic Disease.

Comparative biochemical studies in fibroblasts from patients with different forms of Leigh syndrome

S. Dimauro, F. Santorelli, D. Vivo, 1996, Journal of Inherited Metabolic Disease.

The T9176G mtDNA mutation severely affects ATP production and results in Leigh syndrome

R. Carrozzo, H. Schägger, A. Federico, 2001, Neurology.

Clinical Heterogeneity Associated with the Mitochondrial DNA T8993C Point Mutation

S. Dimauro, F. Santorelli, D. Vivo, 1996, Pediatric Research.