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Article

Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation

23 Nov 2015

Abstract excerpt

The DEPDC5 gene (OMIM #614191), mapped to 22q12.2-q12.3, encodes the DEP domain-containing protein 5. DEPDC5 has been associated with a variety of familial epilepsies, including familial focal epilepsy with variable foci, autosomal dominant nocturnal frontal lobe epilepsy, familial temporal lobe epilepsy, epileptic spasms, and cortical dysplasia.(1-4) Notably, DEPDC5 has never been linked to increased risk of...

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PMID: 27066565
DOI: 10.1212/nxg.0000000000000028

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Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutationPMID 27066565Read ↗

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