Ontology highlight
ABSTRACT:
SUBMITTER: Guner F
PROVIDER: S-EPMC8314181 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
Güner Fabian F Pozner Tatyana T Krach Florian F Prots Iryna I Loskarn Sandra S Schlötzer-Schrehardt Ursula U Winkler Jürgen J Winner Beate B Regensburger Martin M
Frontiers in neuroscience 20210707
Pathogenic variants in <i>SPG11</i> are the most frequent cause of autosomal recessive complicated hereditary spastic paraplegia (HSP). In addition to spastic paraplegia caused by corticospinal degeneration, most patients are significantly affected by progressive weakness and muscle wasting due to alpha motor neuron (MN) degeneration. Mitochondria play a crucial role in neuronal health, and mitochondrial deficits were reported in other types of HSPs. To investigate whether mitochondrial patholog ...[more]