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Mitochondrial disorders v2.45 | SLC25A10 | Arina Puzriakova Mode of inheritance for gene: SLC25A10 was changed from to BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mitochondrial disorders v2.44 | SLC25A10 | Arina Puzriakova Phenotypes for gene: SLC25A10 were changed from to ?Mitochondrial DNA depletion syndrome 19, OMIM:618972 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mitochondrial disorders v1.448 | SLC25A10 | Sarah Leigh Publications for gene: SLC25A10 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mitochondrial disorders v1.423 | SLC25A10 | Sarah Leigh reviewed gene: SLC25A10: Rating: RED; Mode of pathogenicity: ; Publications: 29903433, 29211846 ; Phenotypes: intractable epileptic encephalopathy with complex I deficiency; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Mitochondrial disorders v1.422 | SLC25A10 |
Sarah Leigh gene: SLC25A10 was added gene: SLC25A10 was added to Mitochondrial disorders. Sources: Expert list Mode of inheritance for gene: SLC25A10 was set to |