Ontology highlight
ABSTRACT:
SUBMITTER: Bottani E
PROVIDER: S-EPMC7696526 | biostudies-literature | 2020 Nov
REPOSITORIES: biostudies-literature
Bottani Emanuela E Lamperti Costanza C Prigione Alessandro A Tiranti Valeria V Persico Nicola N Brunetti Dario D
Pharmaceutics 20201111 11
Primary mitochondrial diseases (PMD) refer to a group of severe, often inherited genetic conditions due to mutations in the mitochondrial genome or in the nuclear genes encoding for proteins involved in oxidative phosphorylation (OXPHOS). The mutations hamper the last step of aerobic metabolism, affecting the primary source of cellular ATP synthesis. Mitochondrial diseases are characterized by extremely heterogeneous symptoms, ranging from organ-specific to multisystemic dysfunction with differe ...[more]