Defective mitochondrial adenosine triphosphate production in skeletal muscle from patients with dominant optic atrophy due to OPA1 mutations.
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M. Zeviani | B. Barbiroli | D. Manners | P. Barboni | M. Carbonelli | R. Lodi | C. La Morgia | C. Testa | C. Tonon | E. Malucelli | A. Baruzzi | V. Carelli | R. Liguori | B. Wissinger | M. Valentino | S. Schimpf