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| Childhood onset dystonia, chorea or related movement disorder v0.7 | SUCLG1 |
Ellen McDonagh Source PanelApp was added to SUCLG1. Mode of inheritance for gene SUCLG1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria), 245400 for gene: SUCLG1 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | SUCLG1 |
Ellen McDonagh gene: SUCLG1 was added gene: SUCLG1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: SUCLG1 was set to |
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