Article
Bacterial lipoate protein ligases rescue lipoylation and respiration deficiency in mammals
2024-11-25
Abstract excerpt
<h4>Summary</h4> Human lipoylation pathway deficiencies caused by LIPT2/LIAS/LIPT1 gene mutations lead to inherited metabolic disorders characterized by severe defects of mitochondrial energy and amino acids metabolism. Patients with such mutations suffer from hyperlactic acidemia, encephalopathy, hypotonia and early death. So far there is no effective treatment. Here we introduced the bacteria salvage lipoylatio...
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Identifiers and source
- Literature Corpus work
- 70e87c31-2133-5d34-ae9a-0109a9aa61b4
- DOI
- 10.1101/2024.11.22.624956
