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Possible mitochondrial disorder - nuclear genes v0.5 | VPS13C | Ivone Leong reviewed gene: VPS13C: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Parkinson disease 23, autosomal recessive, early onset, 616840; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Possible mitochondrial disorder - nuclear genes v0.4 | VPS13C |
Ivone Leong gene: VPS13C was added gene: VPS13C was added to Possible mitochondrial disorder - nuclear genes. Sources: Expert Review Red,NHS GMS Mode of inheritance for gene: VPS13C was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: VPS13C were set to Parkinson disease 23, autosomal recessive, early onset, 616840 |