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Childhood onset dystonia, chorea or related movement disorder v0.7 | FOXP2 |
Ellen McDonagh Source PanelApp was added to FOXP2. Mode of inheritance for gene FOXP2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Speech-language disorder-1 602081 for gene: FOXP2 Publications for gene FOXP2 were changed from to 15877281; 22434823; 11586359 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | FOXP2 |
Ellen McDonagh gene: FOXP2 was added gene: FOXP2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: FOXP2 was set to |