The association between SLC25A10 (Solute Carrier Family 25 Member 10) and Mitochondrial Complex I Deficiency, Nuclear Type 1 is supported by expert-curated evidence, drawing on a single expert-curated source, which records likely-pathogenic variants.
Sources1
Clinical variants2
Symptoms96
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.