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| Mitochondrial disorders v1.441 | KIF5A | Sarah Leigh Phenotypes for gene: KIF5A were changed from to Myoclonus, intractable, neonatal 617235; Spastic paraplegia 10, autosomal dominant 604187; {Amyotrophic lateral sclerosis, susceptibility to, 25} 617921 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.441 | KIF5A | Sarah Leigh Publications for gene: KIF5A were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.423 | KIF5A | Sarah Leigh reviewed gene: KIF5A: Rating: RED; Mode of pathogenicity: ; Publications: 29903433; Phenotypes: Myoclonus, intractable, neonatal 617235, Spastic paraplegia 10, autosomal dominant 604187, {Amyotrophic lateral sclerosis, susceptibility to, 25} 617921; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disorders v1.422 | KIF5A |
Sarah Leigh gene: KIF5A was added gene: KIF5A was added to Mitochondrial disorders. Sources: Expert list Mode of inheritance for gene: KIF5A was set to |
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