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| Leukodystrophy v1.0 | ATP7B | Gene migrated from ENSG00000123191 to ENSG00000123191 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Leukodystrophy v0.339 | Bryony Thompson Copied gene ATP7B from panel Leukodystrophy - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Leukodystrophy v0.339 | ATP7B |
Bryony Thompson gene: ATP7B was added gene: ATP7B was added to Leukodystrophy - paediatric. Sources: Expert Review Amber,Expert list Mode of inheritance for gene: ATP7B was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ATP7B were set to 16966556; 12020274 Phenotypes for gene: ATP7B were set to Wilson disease, 277900 |
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