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| Childhood onset dystonia, chorea or related movement disorder v0.7 | INPP5E |
Ellen McDonagh Source PanelApp was added to INPP5E. Mode of inheritance for gene INPP5E was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Joubert syndrome; Joubert syndrome 1 for gene: INPP5E Publications for gene INPP5E were changed from to 26748598; 23386033 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | INPP5E |
Ellen McDonagh gene: INPP5E was added gene: INPP5E was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Red Mode of inheritance for gene: INPP5E was set to |
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