Activity

Filter

Cancel
Date Panel Item Activity
5 actions
Structural basal ganglia disorders v1.19 SERAC1 Arina Puzriakova Phenotypes for gene: SERAC1 were changed from 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, 614739; MEGDEL syndrome; 3-MEthylGlutaconic aciduria, Dystonia-Deafness, Hepatopathy, Encephalopathy, Leigh-like syndrome; MEGDHEL syndrome; Lesions in the basal ganglia to 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome, OMIM:614739; Lesions in the basal ganglia
Structural basal ganglia disorders SERAC1 Louise Daugherty edited their review of SERAC1
Structural basal ganglia disorders SERAC1 Sarah Leigh classified SERAC1 as green
Structural basal ganglia disorders SERAC1 Manju Kurian added SERAC1 to panel
Structural basal ganglia disorders SERAC1 Manju Kurian reviewed SERAC1