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Childhood onset dystonia, chorea or related movement disorder v0.7 | TCTN2 |
Ellen McDonagh Source PanelApp was added to TCTN2. Mode of inheritance for gene TCTN2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Meckel syndrome; Joubert syndrome, Meckel-Gruber syndrome; Joubert syndrome 24 for gene: TCTN2 Publications for gene TCTN2 were changed from to 21565611; 25118024 |
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Childhood onset dystonia, chorea or related movement disorder v0.0 | TCTN2 |
Ellen McDonagh gene: TCTN2 was added gene: TCTN2 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TCTN2 was set to |