The association between NDUFA1 (NADH:Ubiquinone Oxidoreductase Subunit A1) and Mitochondrial Complex I Deficiency, Nuclear Type 1 is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording a causative germline mutation.
Sources2
Clinical variants1
Symptoms96
Compounds0
Trials0
Publications4
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.