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| Childhood onset dystonia, chorea or related movement disorder v0.7 | TMEM107 |
Ellen McDonagh Source PanelApp was added to TMEM107. Mode of inheritance for gene TMEM107 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Orofaciodigital syndrome XVI 617563; ?Joubert syndrome 29 617562; Meckel syndrome 13 617562 for gene: TMEM107 Publications for gene TMEM107 were changed from to 22698544; 26595381; 26123494; 26518474 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | TMEM107 |
Ellen McDonagh gene: TMEM107 was added gene: TMEM107 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: TMEM107 was set to |
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