CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD.
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| Title: | CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. |
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| Authors: | Garibaldi, M.1, Fattori, F.2, Bortolotti, C.3, Brochier, G.4, Labasse, C.4, Verardo, M.2, Bertini, E.2, Pennisi, E.5, Paradas, C.6, Romero, N.4, Antonini, G.1 |
| Source: | Neuromuscular Disorders. Oct2018:Supplement 2, Vol. 28, pS102-S102. 1p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 131609257 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Garibaldi%2C+M%2E%22">Garibaldi, M.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Fattori%2C+F%2E%22">Fattori, F.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Bortolotti%2C+C%2E%22">Bortolotti, C.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Brochier%2C+G%2E%22">Brochier, G.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Labasse%2C+C%2E%22">Labasse, C.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Verardo%2C+M%2E%22">Verardo, M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Bertini%2C+E%2E%22">Bertini, E.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Pennisi%2C+E%2E%22">Pennisi, E.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Paradas%2C+C%2E%22">Paradas, C.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Romero%2C+N%2E%22">Romero, N.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Antonini%2C+G%2E%22">Antonini, G.</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Oct2018:Supplement 2, Vol. 28, pS102-S102. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=131609257 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2018.06.280 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: S102 Titles: – TitleFull: CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Garibaldi, M. – PersonEntity: Name: NameFull: Fattori, F. – PersonEntity: Name: NameFull: Bortolotti, C. – PersonEntity: Name: NameFull: Brochier, G. – PersonEntity: Name: NameFull: Labasse, C. – PersonEntity: Name: NameFull: Verardo, M. – PersonEntity: Name: NameFull: Bertini, E. – PersonEntity: Name: NameFull: Pennisi, E. – PersonEntity: Name: NameFull: Paradas, C. – PersonEntity: Name: NameFull: Romero, N. – PersonEntity: Name: NameFull: Antonini, G. IsPartOfRelationships: – BibEntity: Dates: – D: 02 M: 10 Text: Oct2018:Supplement 2 Type: published Y: 2018 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 28 Titles: – TitleFull: Neuromuscular Disorders Type: main |
| ResultId | 1 |
