Activity
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2 actions
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| Dystonia, chorea or related movement disorder, childhood onset v0.7 | NDUFS8 |
Ellen McDonagh Source PanelApp was added to NDUFS8. Mode of inheritance for gene NDUFS8 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Mitochondrial complex I deficiency, nuclear type 2, 618222 for gene: NDUFS8 |
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| Dystonia, chorea or related movement disorder, childhood onset v0.0 | NDUFS8 |
Ellen McDonagh gene: NDUFS8 was added gene: NDUFS8 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: NDUFS8 was set to |
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