<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ishida S</submitter><funding>European Research Council</funding><pagination>552-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5010101</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>45(5)</volume><pubmed_abstract>The main familial focal epilepsies are autosomal dominant nocturnal frontal lobe epilepsy, familial temporal lobe epilepsy and familial focal epilepsy with variable foci. A frameshift mutation in the DEPDC5 gene (encoding DEP domain-containing protein 5) was identified in a family with focal epilepsy with variable foci by linkage analysis and exome sequencing. Subsequent pyrosequencing of DEPDC5 in a cohort of 15 additional families with focal epilepsies identified 4 nonsense mutations and 1 missense mutation. Our findings provided evidence of frequent (37%) loss-of-function mutations in DEPDC5 associated with a broad spectrum of focal epilepsies. The implication of a DEP (Dishevelled, Egl-10 and Pleckstrin) domain-containing protein that may be involved in membrane trafficking and/or G protein signaling opens new avenues for research.</pubmed_abstract><journal>Nature genetics</journal><pubmed_title>Mutations of DEPDC5 cause autosomal dominant focal epilepsies.</pubmed_title><pmcid>PMC5010101</pmcid><funding_grant_id>322721</funding_grant_id><pubmed_authors>Hirsch E</pubmed_authors><pubmed_authors>Rudolf G</pubmed_authors><pubmed_authors>Picard F</pubmed_authors><pubmed_authors>Genton P</pubmed_authors><pubmed_authors>Mundwiller E</pubmed_authors><pubmed_authors>Wolff M</pubmed_authors><pubmed_authors>Marescaux C</pubmed_authors><pubmed_authors>Achaz G</pubmed_authors><pubmed_authors>Leguern E</pubmed_authors><pubmed_authors>Ishida S</pubmed_authors><pubmed_authors>Baulac M</pubmed_authors><pubmed_authors>Noe E</pubmed_authors><pubmed_authors>Thomas P</pubmed_authors><pubmed_authors>Baulac S</pubmed_authors><pubmed_authors>Miles R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mutations of DEPDC5 cause autosomal dominant focal epilepsies.</name><description>The main familial focal epilepsies are autosomal dominant nocturnal frontal lobe epilepsy, familial temporal lobe epilepsy and familial focal epilepsy with variable foci. A frameshift mutation in the DEPDC5 gene (encoding DEP domain-containing protein 5) was identified in a family with focal epilepsy with variable foci by linkage analysis and exome sequencing. Subsequent pyrosequencing of DEPDC5 in a cohort of 15 additional families with focal epilepsies identified 4 nonsense mutations and 1 missense mutation. Our findings provided evidence of frequent (37%) loss-of-function mutations in DEPDC5 associated with a broad spectrum of focal epilepsies. The implication of a DEP (Dishevelled, Egl-10 and Pleckstrin) domain-containing protein that may be involved in membrane trafficking and/or G protein signaling opens new avenues for research.</description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 May</publication><modification>2020-11-09T08:44:57Z</modification><creation>2019-03-27T02:23:25Z</creation></dates><accession>S-EPMC5010101</accession><cross_references><pubmed>23542701</pubmed><doi>10.1038/ng.2601</doi></cross_references></HashMap>