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Childhood onset dystonia, chorea or related movement disorder v0.7 | SLC20A2 |
Ellen McDonagh Source PanelApp was added to SLC20A2. Mode of inheritance for gene SLC20A2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Basal ganglia calcification, idiopathic, 1 213600; Dystonia for gene: SLC20A2 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | SLC20A2 |
Ellen McDonagh gene: SLC20A2 was added gene: SLC20A2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: SLC20A2 was set to |