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| Childhood onset dystonia, chorea or related movement disorder v0.7 | NDUFS7 |
Ellen McDonagh Source PanelApp was added to NDUFS7. Mode of inheritance for gene NDUFS7 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Mitochondrial complex I deficiency, nuclear type 3, 618224 for gene: NDUFS7 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | NDUFS7 |
Ellen McDonagh gene: NDUFS7 was added gene: NDUFS7 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: NDUFS7 was set to |
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