The association between NDUFB10 (NADH:Ubiquinone Oxidoreductase Subunit B10) and Mitochondrial Complex I Deficiency, Nuclear Type 1 is well established and manually curated, with its 3 contributing sources — 2 of them expert-curated — recording likely-pathogenic variants and a causative germline mutation.
Sources3
Clinical variants1
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.