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| Childhood onset dystonia, chorea or related movement disorder v0.7 | DLAT |
Ellen McDonagh Source PanelApp was added to DLAT. Mode of inheritance for gene DLAT was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Pyruvate dehydrogenase E2 deficiency 245348; Dystonia for gene: DLAT Publications for gene DLAT were changed from to 16049940; 19891062 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | DLAT |
Ellen McDonagh gene: DLAT was added gene: DLAT was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: DLAT was set to |
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