G.P.3.04 Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients
Saved in:
| Title: | G.P.3.04 Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients |
|---|---|
| Authors: | Fratter, C.1, Gorman, G.2, Stewart, J.D.2, Buddles, M.2, Smith, C.1, Evans, J.1, Seller, A.1, Poulton, J.3, Roberts, M.4, Hanna, M.G.5, Rahman, S.6, Omer, S.E.7, Klopstock, T.8, Schoser, B.8, Kornblum, C.9, Lecky, B.10, Chinnery, P.F.2, Turnbull, D.M.2, Horvath, R.2, Taylor, R.W.2 |
| Source: | Neuromuscular Disorders. Sep2009, Vol. 19 Issue 8/9, p562-562. 1p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: asn DbLabel: Academic Search Ultimate An: 43525826 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: G.P.3.04 Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Fratter%2C+C%2E%22">Fratter, C.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Gorman%2C+G%2E%22">Gorman, G.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Stewart%2C+J%2ED%2E%22">Stewart, J.D.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Buddles%2C+M%2E%22">Buddles, M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Smith%2C+C%2E%22">Smith, C.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Evans%2C+J%2E%22">Evans, J.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Seller%2C+A%2E%22">Seller, A.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Poulton%2C+J%2E%22">Poulton, J.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Roberts%2C+M%2E%22">Roberts, M.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Hanna%2C+M%2EG%2E%22">Hanna, M.G.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Rahman%2C+S%2E%22">Rahman, S.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Omer%2C+S%2EE%2E%22">Omer, S.E.</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Klopstock%2C+T%2E%22">Klopstock, T.</searchLink><relatesTo>8</relatesTo><br /><searchLink fieldCode="AR" term="%22Schoser%2C+B%2E%22">Schoser, B.</searchLink><relatesTo>8</relatesTo><br /><searchLink fieldCode="AR" term="%22Kornblum%2C+C%2E%22">Kornblum, C.</searchLink><relatesTo>9</relatesTo><br /><searchLink fieldCode="AR" term="%22Lecky%2C+B%2E%22">Lecky, B.</searchLink><relatesTo>10</relatesTo><br /><searchLink fieldCode="AR" term="%22Chinnery%2C+P%2EF%2E%22">Chinnery, P.F.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Turnbull%2C+D%2EM%2E%22">Turnbull, D.M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Horvath%2C+R%2E%22">Horvath, R.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Taylor%2C+R%2EW%2E%22">Taylor, R.W.</searchLink><relatesTo>2</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Sep2009, Vol. 19 Issue 8/9, p562-562. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=43525826 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2009.06.062 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: 562 Titles: – TitleFull: G.P.3.04 Autosomal dominant Progressive External Ophthalmoplegia (adPEO) due to mutations in the PEO1 gene: A clinical, histochemical and molecular survey of 33 patients Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Fratter, C. – PersonEntity: Name: NameFull: Gorman, G. – PersonEntity: Name: NameFull: Stewart, J.D. – PersonEntity: Name: NameFull: Buddles, M. – PersonEntity: Name: NameFull: Smith, C. – PersonEntity: Name: NameFull: Evans, J. – PersonEntity: Name: NameFull: Seller, A. – PersonEntity: Name: NameFull: Poulton, J. – PersonEntity: Name: NameFull: Roberts, M. – PersonEntity: Name: NameFull: Hanna, M.G. – PersonEntity: Name: NameFull: Rahman, S. – PersonEntity: Name: NameFull: Omer, S.E. – PersonEntity: Name: NameFull: Klopstock, T. – PersonEntity: Name: NameFull: Schoser, B. – PersonEntity: Name: NameFull: Kornblum, C. – PersonEntity: Name: NameFull: Lecky, B. – PersonEntity: Name: NameFull: Chinnery, P.F. – PersonEntity: Name: NameFull: Turnbull, D.M. – PersonEntity: Name: NameFull: Horvath, R. – PersonEntity: Name: NameFull: Taylor, R.W. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: Sep2009 Type: published Y: 2009 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 19 – Type: issue Value: 8/9 Titles: – TitleFull: Neuromuscular Disorders Type: main |
| ResultId | 1 |