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| Childhood onset dystonia, chorea or related movement disorder v0.7 | NKX6-2 |
Ellen McDonagh Source PanelApp was added to NKX6-2. Mode of inheritance for gene NKX6-2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy 617560 for gene: NKX6-2 Publications for gene NKX6-2 were changed from to 15601927; 28575651 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | NKX6-2 |
Ellen McDonagh gene: NKX6-2 was added gene: NKX6-2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: NKX6-2 was set to |
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