About: Mutations of DEPDC5 cause autosomal dominant focal epilepsies

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scientific article published on 31 March 2013

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2013 (ast) наукова стаття, опублікована в березні 2013 (uk) مقالة علمية نشرت في 31 مارس 2013 (ar) scientific article published on 31 March 2013 (en)
publication date	wds:Q37229691-8B7512BD-E6B3-4732-A906-EE78E5A20664
publication date	2013-03-31 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q37229691-ABE703EE-9BDB-4778-AA30-BBAA37E57469
language of work or name	English
exact match	wds:Q37229691-BEDCC6EA-3E7C-442C-8726-27AFE6B74182
exact match	https://scigraph.springernature.com/pub.10.1038/ng.2601
cites work	wds:Q37229691-0209BDD6-9534-40D9-87CD-FD08BCCBFA3D wds:Q37229691-1B3012D1-B5B4-4741-B9B9-E883E401B344 wds:Q37229691-1C11EE98-EF92-4455-96C3-2936A0B65CAA wds:Q37229691-2B79EEB0-AB7E-4DB8-93CF-7AA9F2EFA7ED wds:Q37229691-30D6B5BD-EB79-4417-BDEE-EACD6ADDDE72 wds:Q37229691-37D3DDE8-C9C0-4312-AF3C-8FA74CE9024F wds:Q37229691-46F6BA46-C799-4138-AB3F-C67961019605 wds:Q37229691-62DDA991-C88F-41D1-900E-8AEB30B8296E wds:Q37229691-631B9813-F1EE-4B7A-BD72-8991B4940282 wds:Q37229691-69E8753D-AC40-419D-950A-320BF11B4F10 wds:Q37229691-76CCB63F-88ED-4A53-9DD2-55110406955C wds:Q37229691-88F5CBC5-43D7-4FC8-B289-5DDD9732009C wds:Q37229691-ACA46598-582F-4BCD-91FC-6F573B34FD7F wds:Q37229691-C38A0F83-076D-4DD5-9550-BFF4DF2854D3 wds:Q37229691-C6E5BFCC-8441-4295-B5F1-DF930036CCD2 wds:Q37229691-D475F471-5A02-4F22-B999-C8D8058880FD wds:Q37229691-D8C7215D-9020-44A6-9BAE-87DF549A1CFF wds:Q37229691-D9A36A4F-586D-4851-ACC5-027D9F837A3E
cites work	Dominant partial epilepsies: A clinical, electrophysiological and genetic study of 19 European families Familial temporal lobe epilepsy: a common disorder identified in twins Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder Complex chromosome 22 rearrangements in astrocytic tumors identified using microsatellite and chromosome 22 tile path array analysis Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro Localization of a gene for partial epilepsy to chromosome 10q Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12. Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12 Advances on the Genetics of Mendelian Idiopathic Epilepsies A conserved coatomer-related complex containing Sec13 and Seh1 dynamically associates with the vacuole in Saccharomyces cerevisiae Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy Familial partial epilepsy with variable foci: a new family with suggestion of linkage to chromosome 22q12. Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum [Autosomal dominant nocturnal frontal lobe epilepsy] Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2 Familial partial epilepsy with variable foci in a Dutch family: clinical characteristics and confirmation of linkage to chromosome 22q
author name string	wds:Q37229691-207BF80C-0B0B-43BB-9DC8-67793003B554 wds:Q37229691-4AD03D00-366C-47D4-A3CB-79CCB3A8B47A wds:Q37229691-4ADBA08D-4401-4B61-8F41-ADCFD1EF1946 wds:Q37229691-50D17720-A1EE-467B-817F-2163E0F735B3 wds:Q37229691-619A1536-A739-4D67-B423-131EFD9BC2D3 wds:Q37229691-69550A0F-29CD-4D6A-8E46-71A75AA5BD71 wds:Q37229691-A6F11375-8051-4EA1-A836-64EA4664B1D0 wds:Q37229691-A79CDC74-3B21-45AD-A031-EE682E75A1ED wds:Q37229691-B2DCB4CC-731A-4142-8CAA-ECDB1D71CE98 wds:Q37229691-B413E6D6-8774-4AFD-9427-2207CE25AB36 wds:Q37229691-B4AF06F1-3DF8-4F06-BF9B-A605ED9FB76A wds:Q37229691-D7FF4168-6B38-4F8A-8D7F-F6DAB34EF5F6
author name string	Pierre Genton Emeline Mundwiller Fabienne Picard Pierre Thomas Markus Wolff Christian Marescaux Edouard Hirsch Guillaume Achaz Eric Leguern Eric Noé Richard Miles Saeko Ishida
rdfs:label	Mutations of DEPDC5 cause autosomal dominant focal epilepsies. (nl) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (en) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (ast)
skos:prefLabel	Mutations of DEPDC5 cause autosomal dominant focal epilepsies. (nl) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (en) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (ast)
name	Mutations of DEPDC5 cause autosomal dominant focal epilepsies. (nl) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (en) Mutations of DEPDC5 cause autosomal dominant focal epilepsies (ast)
author	wds:Q37229691-594E52D4-A067-4885-A2E7-106136109FF3 wds:Q37229691-5D10731C-05EC-42B4-86D8-A508DAF9246E wds:Q37229691-FBEB7BFA-1297-4409-8A28-7AD53ADE1D00
author	Stéphanie Baulac Gabrielle Rudolf Michel Baulac
title	wds:Q37229691-1ABE7524-C720-455A-8E3B-B36D452040E6
title	Mutations of DEPDC5 cause autosomal dominant focal epilepsies (en)

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