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EPM2AIP1

Official Full Name
EPM2A interacting protein 1
Organism
Homo sapiens
GeneID
9852
Background
The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]

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