SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype.
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| Title: | SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype. |
|---|---|
| Authors: | Bugiardini, E.1, Rivolta, I.2, Binda, A.2, Soriano Caminero, A.3, Cirillo, F.4, Cinti, A.5, Giovannoni, R.5, Botta, A.6, Cardani, R.7, Wicklund, M.P.3, Meola, G.1,7 giovanni.meola@unimi.it |
| Source: | Neuromuscular Disorders. Apr2015, Vol. 25 Issue 4, p301-307. 7p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 101930912 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Bugiardini%2C+E%2E%22">Bugiardini, E.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Rivolta%2C+I%2E%22">Rivolta, I.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Binda%2C+A%2E%22">Binda, A.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Soriano+Caminero%2C+A%2E%22">Soriano Caminero, A.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Cirillo%2C+F%2E%22">Cirillo, F.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Cinti%2C+A%2E%22">Cinti, A.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Giovannoni%2C+R%2E%22">Giovannoni, R.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Botta%2C+A%2E%22">Botta, A.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Cardani%2C+R%2E%22">Cardani, R.</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Wicklund%2C+M%2EP%2E%22">Wicklund, M.P.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Meola%2C+G%2E%22">Meola, G.</searchLink><relatesTo>1,7</relatesTo><i> giovanni.meola@unimi.it</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Apr2015, Vol. 25 Issue 4, p301-307. 7p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=101930912 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2015.01.006 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 301 Titles: – TitleFull: SCN4A mutation as modifying factor of Myotonic Dystrophy Type 2 phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Bugiardini, E. – PersonEntity: Name: NameFull: Rivolta, I. – PersonEntity: Name: NameFull: Binda, A. – PersonEntity: Name: NameFull: Soriano Caminero, A. – PersonEntity: Name: NameFull: Cirillo, F. – PersonEntity: Name: NameFull: Cinti, A. – PersonEntity: Name: NameFull: Giovannoni, R. – PersonEntity: Name: NameFull: Botta, A. – PersonEntity: Name: NameFull: Cardani, R. – PersonEntity: Name: NameFull: Wicklund, M.P. – PersonEntity: Name: NameFull: Meola, G. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 04 Text: Apr2015 Type: published Y: 2015 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 25 – Type: issue Value: 4 Titles: – TitleFull: Neuromuscular Disorders Type: main |
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