Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy.
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| Title: | Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy. |
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| Authors: | Poulton J (AUTHOR), Jayawant S (AUTHOR), O'Rourke A (AUTHOR), Morten K (AUTHOR), Ashley N (AUTHOR), Narasimhan M (AUTHOR), Fratter C (AUTHOR) |
| Source: | Developmental Medicine & Child Neurology. Jan2007 Supplement 108, Vol. 49, p10-10. 1p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 105545655 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=105545655 |
| RecordInfo | BibRecord: BibEntity: Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: 10 Titles: – TitleFull: Mutations in the mitochondrial DNA gamma polymerase (POLG) may cause Alpers syndrome, mitochondrial DNA depletion, and non-syndromic status epilepticus: implications for valproate therapy. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Poulton J – PersonEntity: Name: NameFull: Jayawant S – PersonEntity: Name: NameFull: O'Rourke A – PersonEntity: Name: NameFull: Morten K – PersonEntity: Name: NameFull: Ashley N – PersonEntity: Name: NameFull: Narasimhan M – PersonEntity: Name: NameFull: Fratter C IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 01 Text: Jan2007 Supplement 108 Type: published Y: 2007 Identifiers: – Type: issn-print Value: 00121622 Numbering: – Type: volume Value: 49 Titles: – TitleFull: Developmental Medicine & Child Neurology Type: main |
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