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| Childhood onset dystonia, chorea or related movement disorder v0.7 | HYLS1 |
Ellen McDonagh Source PanelApp was added to HYLS1. Mode of inheritance for gene HYLS1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome; Hydrolethalus syndrome, 236680 for gene: HYLS1 Publications for gene HYLS1 were changed from to 18648327 - Hydrolethalus syndrome; 19656802 - impairment in ciligenesis; 15843405 - Hydrolethalus syndrome; 26830932 - report in two siblings with Joubert syndrome |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | HYLS1 |
Ellen McDonagh gene: HYLS1 was added gene: HYLS1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: HYLS1 was set to |
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