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autosomal dominant Parkinson's disease 8 (DOID:0060371)
Alliance: disease page
Synonyms: autosomal dominant Parkinson disease 8
Alt IDs: OMIM:607060
Definition: A Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene (LRRK2) on chromosome 12q12.

Disease References using Mouse Models (11)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory