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| Childhood onset dystonia, chorea or related movement disorder v0.7 | PDE10A |
Ellen McDonagh Source PanelApp was added to PDE10A. Mode of inheritance for gene PDE10A was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Striatal degeneration, autosomal dominant 616922; Dyskinesia, limb and orofacial, infantile-onset 616921 for gene: PDE10A Publications for gene PDE10A were changed from to 27058447; 27058446 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | PDE10A |
Ellen McDonagh gene: PDE10A was added gene: PDE10A was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: PDE10A was set to |
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