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Human Disease and Mouse Model Detail
Human Disease Spinocerebellar Ataxia, Autosomal Recessive 4; SCAR4
OMIM ID: 607317
Synonyms Spinocerebellar Ataxia; Spinocerebellar Ataxia 24, Formerly; SCA24, FORMERLY; Spinocerebellar Ataxia with Saccadic Intrusions; SCASI
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/16/2014
MGI 5.20
The Jackson Laboratory