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| Childhood onset dystonia, chorea or related movement disorder v0.7 | NDUFA9 |
Ellen McDonagh Source PanelApp was added to NDUFA9. Added phenotypes Leigh syndrome due to mitochondrial complex I deficiency 256000 for gene: NDUFA9 Publications for gene NDUFA9 were changed from to 22114105 |
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| Childhood onset dystonia, chorea or related movement disorder v0.1 | NDUFA9 |
Ellen McDonagh gene: NDUFA9 was added gene: NDUFA9 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: South West GLH Mode of inheritance for gene: NDUFA9 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: NDUFA9 were set to Mitochondrial complex I deficiency, nuclear type 26, 618247 |
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