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| Childhood onset dystonia, chorea or related movement disorder v0.7 | TCTN3 |
Ellen McDonagh Source PanelApp was added to TCTN3. Mode of inheritance for gene TCTN3 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Meckel-Gruber; Joubert syndrome; Joubert syndrome 18; Orofaciodigital syndrome IV; Mohr-Majewski syndrome for gene: TCTN3 Publications for gene TCTN3 were changed from to 22883145; 25118024 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | TCTN3 |
Ellen McDonagh gene: TCTN3 was added gene: TCTN3 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TCTN3 was set to |
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