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Multisystem manifestations of mitochondrial disorders
Stefano Di Donato
Fondazione IRCCS Istituto Neurologico "C. Besta"
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Medicine & Life Sciences
Mitochondrial Diseases
100%
Oxidative Phosphorylation
90%
Mitochondrial DNA
56%
Inborn Genetic Diseases
49%
Autosomal Dominant Optic Atrophy
42%
Leber's Hereditary Optic Atrophy
39%
Endocrine System
32%
Mutation
29%
DNA
29%
Electron Transport
29%
Eukaryotic Cells
28%
Muscular Diseases
28%
Genetic Association Studies
28%
Peripheral Nervous System Diseases
28%
Optic Nerve
27%
Organelles
25%
Age of Onset
25%
Gastrointestinal Tract
23%
Signs and Symptoms
23%
Mitochondria
22%
Central Nervous System
19%
Heart
17%
Pathology
16%
Apoptosis
16%
Kidney
14%
Liver
13%