RGD Annotation Report for progressive myoclonus epilepsy 1ARat Genome Database

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An association has been curated linking CSTB and progressive myoclonus epilepsy 1A in Pan paniscus.

The association was inferred from sequence orthology (ISO)
The annotation was made from OMIM Disease Annotation Pipeline
The annotation has been inferred from sequence orthology with CSTB (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
1 RGD objects have been annotated to progressive myoclonus epilepsy 1A (DOID:0111452)
0 papers in RGD have been used to annotate CSTB

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.