C. R. Barrionuevo

Characterization of six mutations in five Spanish patients with mitochondrial acetoacetyl-CoA thiolase deficiency: effects of amino acid substitutions on tertiary structure.

Haruki Nakamura, C. Pérez-Cerdá, M. Ugarte, 2002, Molecular genetics and metabolism.

Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.

J. Arenas, Y. Campos, A. Cabello, 1995, Pediatric neurology.