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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.
A930003G21Rik; EPM2A (laforin) interacting protein 1; EPM2A interacting protein 1; EPM2A-interacting protein 1; EPM2AIP1; KIAA0766; Laforin-interacting protein; mKIAA0766; My007
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