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| Hereditary Spastic Paraplegia v2.0 | FBXO7 | Gene migrated from ENSG00000100225 to ENSG00000100225 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia v1.114 | Bryony Thompson Copied gene FBXO7 from panel Hereditary Spastic Paraplegia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia v1.114 | FBXO7 |
Bryony Thompson gene: FBXO7 was added gene: FBXO7 was added to Hereditary Spastic Paraplegia. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: FBXO7 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: FBXO7 were set to 18513678; 19038853 Phenotypes for gene: FBXO7 were set to Parkinson disease 15, autosomal recessive MIM#260300 |
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