Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3.
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| Title: | Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3. |
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| Authors: | Korenke GC; Pediatrics Hospital, Klinikum Oldenburg, Oldenburg, Germany., Eggert M; Institute of Human Genetics, Ludwig-Maximilians-University Hospital, Munich, Germany., Thiele H; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany., Nürnberg P; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany., Sander T; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany., Steinlein OK; Institute of Human Genetics, Ludwig-Maximilians-University Hospital, Munich, Germany. |
| Source: | Epilepsia [Epilepsia] 2016 Mar; Vol. 57 (3), pp. e60-3. Date of Electronic Publication: 2016 Jan 20. |
| Publication Type: | Case Reports; Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Blackwell Science Country of Publication: United States NLM ID: 2983306R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1528-1167 (Electronic) Linking ISSN: 00139580 NLM ISO Abbreviation: Epilepsia Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 26786403 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Korenke+GC%22">Korenke GC</searchLink>; Pediatrics Hospital, Klinikum Oldenburg, Oldenburg, Germany.<br /><searchLink fieldCode="AU" term="%22Eggert+M%22">Eggert M</searchLink>; Institute of Human Genetics, Ludwig-Maximilians-University Hospital, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Thiele+H%22">Thiele H</searchLink>; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.<br /><searchLink fieldCode="AU" term="%22Nürnberg+P%22">Nürnberg P</searchLink>; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.; Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.; Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), University of Cologne, Cologne, Germany.<br /><searchLink fieldCode="AU" term="%22Sander+T%22">Sander T</searchLink>; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.<br /><searchLink fieldCode="AU" term="%22Steinlein+OK%22">Steinlein OK</searchLink>; Institute of Human Genetics, Ludwig-Maximilians-University Hospital, Munich, Germany. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%222983306R%22">Epilepsia</searchLink> [Epilepsia] 2016 Mar; Vol. 57 (3), pp. e60-3. <i>Date of Electronic Publication: </i>2016 Jan 20. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Blackwell+Science%22">Blackwell Science </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>2983306R <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1528-1167 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200139580%22">00139580 </searchLink><i>NLM ISO Abbreviation: </i>Epilepsia <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=26786403 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/epi.13307 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: e60 Titles: – TitleFull: Nocturnal frontal lobe epilepsy caused by a mutation in the GATOR1 complex gene NPRL3. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Korenke GC – PersonEntity: Name: NameFull: Eggert M – PersonEntity: Name: NameFull: Thiele H – PersonEntity: Name: NameFull: Nürnberg P – PersonEntity: Name: NameFull: Sander T – PersonEntity: Name: NameFull: Steinlein OK IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2016 Mar Type: published Y: 2016 Identifiers: – Type: issn-electronic Value: 1528-1167 Numbering: – Type: volume Value: 57 – Type: issue Value: 3 Titles: – TitleFull: Epilepsia Type: main |
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