Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene.
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| Title: | Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene. |
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| Authors: | Li, Shao1 (AUTHOR) kedalishao@163.com, Shang, Dandan1 (AUTHOR), Du, Yanjiao1 (AUTHOR), Li, Yan1 (AUTHOR), Liu, Ruihua1 (AUTHOR) |
| Source: | BMC Neurology. 6/26/2023, Vol. 23 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 164551316 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Li%2C+Shao%22">Li, Shao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> kedalishao@163.com</i><br /><searchLink fieldCode="AR" term="%22Shang%2C+Dandan%22">Shang, Dandan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Du%2C+Yanjiao%22">Du, Yanjiao</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Li%2C+Yan%22">Li, Yan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Liu%2C+Ruihua%22">Liu, Ruihua</searchLink><relatesTo>1</relatesTo> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22BMC+Neurology%22">BMC Neurology</searchLink>. 6/26/2023, Vol. 23 Issue 1, p1-5. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=164551316 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12883-023-03304-5 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Li, Shao – PersonEntity: Name: NameFull: Shang, Dandan – PersonEntity: Name: NameFull: Du, Yanjiao – PersonEntity: Name: NameFull: Li, Yan – PersonEntity: Name: NameFull: Liu, Ruihua IsPartOfRelationships: – BibEntity: Dates: – D: 26 M: 06 Text: 6/26/2023 Type: published Y: 2023 Identifiers: – Type: issn-print Value: 14712377 Numbering: – Type: volume Value: 23 – Type: issue Value: 1 Titles: – TitleFull: BMC Neurology Type: main |
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