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Childhood onset dystonia, chorea or related movement disorder v0.7 | ATP1A2 |
Ellen McDonagh Source PanelApp was added to ATP1A2. Mode of inheritance for gene ATP1A2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes familial basilar migraine 602481; familial hemiplegic migraine type 2, 602481; alternating hemiplegia of childhood 104290; Dystonia; migraine for gene: ATP1A2 Publications for gene ATP1A2 were changed from to 18056581; 12953268; 12539047 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | ATP1A2 |
Ellen McDonagh gene: ATP1A2 was added gene: ATP1A2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: ATP1A2 was set to |