P55 Reversible infantile respiratory chain deficiency is a genetically heterogenous mitochondrial disease
Saved in:
| Title: | P55 Reversible infantile respiratory chain deficiency is a genetically heterogenous mitochondrial disease |
|---|---|
| Authors: | Uusimaa, J., Jungbluth, H., Fratter, C., Bailey, E.M. Fernandez-Vizarra, Crisponi, B.G., Feng, L., Zeviani, M., Hughes, I., Treacy, E., Birks, J., Brown, G.K., Sewry, C., Muntoni, F., Poulton, J. |
| Source: | Neuromuscular Disorders. Mar2011 Supplement 1, Vol. 21, pS22-S22. 1p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 59801215 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: P55 Reversible infantile respiratory chain deficiency is a genetically heterogenous mitochondrial disease – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Uusimaa%2C+J%2E%22">Uusimaa, J.</searchLink><br /><searchLink fieldCode="AR" term="%22Jungbluth%2C+H%2E%22">Jungbluth, H.</searchLink><br /><searchLink fieldCode="AR" term="%22Fratter%2C+C%2E%22">Fratter, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Bailey%2C+E%2EM%2E+Fernandez-Vizarra%22">Bailey, E.M. Fernandez-Vizarra</searchLink><br /><searchLink fieldCode="AR" term="%22Crisponi%2C+B%2EG%2E%22">Crisponi, B.G.</searchLink><br /><searchLink fieldCode="AR" term="%22Feng%2C+L%2E%22">Feng, L.</searchLink><br /><searchLink fieldCode="AR" term="%22Zeviani%2C+M%2E%22">Zeviani, M.</searchLink><br /><searchLink fieldCode="AR" term="%22Hughes%2C+I%2E%22">Hughes, I.</searchLink><br /><searchLink fieldCode="AR" term="%22Treacy%2C+E%2E%22">Treacy, E.</searchLink><br /><searchLink fieldCode="AR" term="%22Birks%2C+J%2E%22">Birks, J.</searchLink><br /><searchLink fieldCode="AR" term="%22Brown%2C+G%2EK%2E%22">Brown, G.K.</searchLink><br /><searchLink fieldCode="AR" term="%22Sewry%2C+C%2E%22">Sewry, C.</searchLink><br /><searchLink fieldCode="AR" term="%22Muntoni%2C+F%2E%22">Muntoni, F.</searchLink><br /><searchLink fieldCode="AR" term="%22Poulton%2C+J%2E%22">Poulton, J.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Mar2011 Supplement 1, Vol. 21, pS22-S22. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=59801215 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/S0960-8966(11)70074-8 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: S22 Titles: – TitleFull: P55 Reversible infantile respiratory chain deficiency is a genetically heterogenous mitochondrial disease Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Uusimaa, J. – PersonEntity: Name: NameFull: Jungbluth, H. – PersonEntity: Name: NameFull: Fratter, C. – PersonEntity: Name: NameFull: Bailey, E.M. Fernandez-Vizarra – PersonEntity: Name: NameFull: Crisponi, B.G. – PersonEntity: Name: NameFull: Feng, L. – PersonEntity: Name: NameFull: Zeviani, M. – PersonEntity: Name: NameFull: Hughes, I. – PersonEntity: Name: NameFull: Treacy, E. – PersonEntity: Name: NameFull: Birks, J. – PersonEntity: Name: NameFull: Brown, G.K. – PersonEntity: Name: NameFull: Sewry, C. – PersonEntity: Name: NameFull: Muntoni, F. – PersonEntity: Name: NameFull: Poulton, J. IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 03 Text: Mar2011 Supplement 1 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 21 Titles: – TitleFull: Neuromuscular Disorders Type: main |
| ResultId | 1 |
