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A biochemical deficiency of mitochondrial complex I (CI) underlies ~30% of cases of primary mitochondrial disease, yet the inventory of molecular machinery required for CI assembly remains incomplete. We previously characterised patients with isolated CI deficiency caused by segregating variants in ...
ORGANISM(S): Homo sapiens (Human) 
2025-08-08 | PXD055511 | Pride
Here we used complexome profiling to characterize the functional consequences of RTN4IP1 mutations in RTN4IP1 cells.
ORGANISM(S): Homo sapiens (Human) 
2025-08-08 | PXD064861 | Pride
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