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| Childhood onset dystonia, chorea or related movement disorder v0.7 | NDUFAF2 |
Ellen McDonagh Source PanelApp was added to NDUFAF2. Mode of inheritance for gene NDUFAF2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Mitochondrial complex I deficiency, nuclear type 10, 618233 for gene: NDUFAF2 Publications for gene NDUFAF2 were changed from to 16200211; 20818383; 20571988 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | NDUFAF2 |
Ellen McDonagh gene: NDUFAF2 was added gene: NDUFAF2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: NDUFAF2 was set to |
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