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Structural basal ganglia disorders v1.12 NDUFA1 Ellen McDonagh Added comment: Comment on mode of inheritance: Changed from 'Both monoallelic and biallelic' to X-linked, as encoded on the X-chromosome.
Structural basal ganglia disorders v1.12 NDUFA1 Ellen McDonagh Mode of inheritance for gene: NDUFA1 was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Structural basal ganglia disorders NDUFA10 Sarah Leigh classified NDUFA10 as green
Structural basal ganglia disorders NDUFA10 Sarah Leigh marked NDUFA10 as ready
Structural basal ganglia disorders NDUFA10 Sarah Leigh commented on NDUFA10
Structural basal ganglia disorders NDUFA1 Sarah Leigh edited their review of NDUFA1
Structural basal ganglia disorders NDUFA1 Sarah Leigh classified NDUFA1 as green
Structural basal ganglia disorders NDUFA1 Sarah Leigh commented on NDUFA1
Structural basal ganglia disorders NDUFA1 Manju Kurian added NDUFA1 to panel
Structural basal ganglia disorders NDUFA1 Manju Kurian reviewed NDUFA1
Structural basal ganglia disorders NDUFA10 Manju Kurian added NDUFA10 to panel
Structural basal ganglia disorders NDUFA10 Manju Kurian reviewed NDUFA10