De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy.
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| Title: | De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. |
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| Authors: | Stringer, Robin N.1,2 (AUTHOR), Jurkovicova-Tarabova, Bohumila3 (AUTHOR), Souza, Ivana A.4 (AUTHOR), Ibrahim, Judy5 (AUTHOR), Vacik, Tomas6 (AUTHOR), Fathalla, Waseem Mahmoud7 (AUTHOR), Hertecant, Jozef5,8 (AUTHOR), Zamponi, Gerald W.4 (AUTHOR), Lacinova, Lubica3 (AUTHOR), Weiss, Norbert1,2,3,6 (AUTHOR) nalweiss@gmail.com |
| Source: | Molecular Brain. 8/16/2021, Vol. 14 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 152013038 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Stringer%2C+Robin+N%2E%22">Stringer, Robin N.</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Jurkovicova-Tarabova%2C+Bohumila%22">Jurkovicova-Tarabova, Bohumila</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Souza%2C+Ivana+A%2E%22">Souza, Ivana A.</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ibrahim%2C+Judy%22">Ibrahim, Judy</searchLink><relatesTo>5</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Vacik%2C+Tomas%22">Vacik, Tomas</searchLink><relatesTo>6</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Fathalla%2C+Waseem+Mahmoud%22">Fathalla, Waseem Mahmoud</searchLink><relatesTo>7</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hertecant%2C+Jozef%22">Hertecant, Jozef</searchLink><relatesTo>5,8</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zamponi%2C+Gerald+W%2E%22">Zamponi, Gerald W.</searchLink><relatesTo>4</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Lacinova%2C+Lubica%22">Lacinova, Lubica</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Weiss%2C+Norbert%22">Weiss, Norbert</searchLink><relatesTo>1,2,3,6</relatesTo> (AUTHOR)<i> nalweiss@gmail.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Molecular+Brain%22">Molecular Brain</searchLink>. 8/16/2021, Vol. 14 Issue 1, p1-5. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=152013038 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13041-021-00838-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: De novo SCN8A and inherited rare CACNA1H variants associated with severe developmental and epileptic encephalopathy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Stringer, Robin N. – PersonEntity: Name: NameFull: Jurkovicova-Tarabova, Bohumila – PersonEntity: Name: NameFull: Souza, Ivana A. – PersonEntity: Name: NameFull: Ibrahim, Judy – PersonEntity: Name: NameFull: Vacik, Tomas – PersonEntity: Name: NameFull: Fathalla, Waseem Mahmoud – PersonEntity: Name: NameFull: Hertecant, Jozef – PersonEntity: Name: NameFull: Zamponi, Gerald W. – PersonEntity: Name: NameFull: Lacinova, Lubica – PersonEntity: Name: NameFull: Weiss, Norbert IsPartOfRelationships: – BibEntity: Dates: – D: 16 M: 08 Text: 8/16/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 17566606 Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: Molecular Brain Type: main |
| ResultId | 1 |