| Human Disease |
Kufor-Rakeb Syndrome; KRS OMIM ID: 606693 |
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| Synonyms | Pallidopyramidal Degeneration with Supranuclear Upgaze Paresis and Dementia; KRPPD; Parkinson Disease 9, Autosomal Recessive; PARK9 | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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