| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Mitochondrial disease v2.1 | Lucy Spencer Copied gene SLC16A13 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v2.1 | SLC16A13 |
Lucy Spencer gene: SLC16A13 was added gene: SLC16A13 was added to Mitochondrial disease. Sources: Literature Mode of inheritance for gene: SLC16A13 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SLC16A13 were set to 42173862 Phenotypes for gene: SLC16A13 were set to Lactic acidosis MONDO:0006040, SLC16A13-related |
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