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| Childhood onset dystonia, chorea or related movement disorder v0.7 | FOLR1 |
Ellen McDonagh Source PanelApp was added to FOLR1. Mode of inheritance for gene FOLR1 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Neurodegeneration due to cerebral folate transport deficiency, 613068; Folate receptor alpha deficiency for gene: FOLR1 Publications for gene FOLR1 were changed from to 27830117; 21937992; 19732866; 2044715 |
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| Childhood onset dystonia, chorea or related movement disorder v0.0 | FOLR1 |
Ellen McDonagh gene: FOLR1 was added gene: FOLR1 was added to Childhood onset dystonia or chorea or related movement disorder. Sources: London North GLH,Expert Review Green Mode of inheritance for gene: FOLR1 was set to |
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