RGD Annotation Report for childhood absence epilepsyRat Genome Database

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An association has been curated linking HCN1 and childhood absence epilepsy in Homo sapiens.

The association was inferred from sequence orthology (ISO)
The annotation was made from Strauss U, etal., Eur J Neurosci. 2004 Jun;19(11):3048-58.
The annotation has been inferred from sequence orthology with Hcn1 (Rattus norvegicus) [(IEP) inferred from expression pattern]
2 additional annotations were made from Strauss U, etal., Eur J Neurosci. 2004 Jun;19(11):3048-58.
36 RGD objects have been annotated to childhood absence epilepsy (DOID:1825)
20 papers in RGD have been used to annotate HCN1

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