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| Childhood onset dystonia, chorea or related movement disorder v0.7 | MAOA |
Ellen McDonagh Source PanelApp was added to MAOA. Mode of inheritance for gene MAOA was changed from to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) Added phenotypes Brunner syndrome, 300615; Monoamine oxidase A deficiency for gene: MAOA Publications for gene MAOA were changed from to 8211186; 27830117; 24169519 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | MAOA |
Ellen McDonagh gene: MAOA was added gene: MAOA was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: MAOA was set to |
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