Homoplasmy of a mitochondrial 3697G>A mutation causes Leigh syndrome

NDUFA4 Is a Subunit of Complex IV of the Mammalian Electron Transport Chain

(2012) Eduardo Balsa et al.   Cell Metabolism

The implications of mitochondrial DNA copy number regulation during embryogenesis

(2011) Phillippa J. Carling et al.   MITOCHONDRION

Structure of the membrane domain of respiratory complex I

(2011) Rouslan G. Efremov et al.   NATURE

Reversible infantile respiratory chain deficiency: A clinical and molecular study

(2010) Masakazu Mimaki et al.   ANNALS OF NEUROLOGY

PROTON SPECTROSCOPY IN FIVE PATIENTS WITH LEIGH'S DISEASE AND MITOCHONDRIAL ENZYME DEFICIENCY

(2010) Ingeborg Krägeloh-Mann et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Identification of novel mutations in five patients with mitochondrial encephalomyopathy

(2008) Lucia Valente et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS