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| Ataxia v2.0 | NOL3 | Gene migrated from ENSG00000140939 to ENSG00000140939 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.97 | Bryony Thompson Copied gene NOL3 from panel Ataxia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ataxia v1.97 | NOL3 |
Bryony Thompson gene: NOL3 was added gene: NOL3 was added to Ataxia. Sources: Expert Review Red,Royal Melbourne Hospital Mode of inheritance for gene: NOL3 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: NOL3 were set to 22926851 Phenotypes for gene: NOL3 were set to Myoclonus, familial cortical |
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