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| Childhood onset dystonia, chorea or related movement disorder v0.1 | MAT1A |
Ellen McDonagh Source South West GLH was added to MAT1A. Mode of inheritance for gene MAT1A was changed from to Unknown Added phenotypes Hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency, 250850 for gene: MAT1A |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | MAT1A |
Ellen McDonagh gene: MAT1A was added gene: MAT1A was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: MAT1A was set to |
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