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Structural basal ganglia disorders v1.32 C19orf12 Sarah Leigh Phenotypes for gene: C19orf12 were changed from to ?Spastic paraplegia 43, autosomal recessive, OMIM:615043; Neurodegeneration with brain iron accumulation 4, OMIM: 614298
Structural basal ganglia disorders v1.31 C19orf12 Sarah Leigh Publications for gene: C19orf12 were set to
Structural basal ganglia disorders C19orf12 Sarah Leigh classified C19orf12 as green
Structural basal ganglia disorders C19orf12 Manju Kurian added C19orf12 to panel
Structural basal ganglia disorders C19orf12 Manju Kurian reviewed C19orf12