Activity
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2 actions
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| Dystonia, chorea or related movement disorder, childhood onset v0.7 | KCNQ3 |
Ellen McDonagh Source PanelApp was added to KCNQ3. Mode of inheritance for gene KCNQ3 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Added phenotypes Seizures, benign neonatal, type 2, 121201 for gene: KCNQ3 |
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| Dystonia, chorea or related movement disorder, childhood onset v0.0 | KCNQ3 |
Ellen McDonagh gene: KCNQ3 was added gene: KCNQ3 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: KCNQ3 was set to |
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