G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features.
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| Title: | G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features. |
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| Authors: | Ben Yaou, R.1, Gerard, M.2, Chami, K.3, Sehier, A.2, Belin, A.4, Labombarda, F.4, Richard, P.5, Bonne, G.6, Leturcq, F.7, Chapon, F.4 |
| Source: | Neuromuscular Disorders. Oct2014, Vol. 24 Issue 9/10, p843-844. 2p. |
| Database: | Academic Search Ultimate |
| FullText | Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 97955578 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Ben+Yaou%2C+R%2E%22">Ben Yaou, R.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Gerard%2C+M%2E%22">Gerard, M.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Chami%2C+K%2E%22">Chami, K.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Sehier%2C+A%2E%22">Sehier, A.</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Belin%2C+A%2E%22">Belin, A.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Labombarda%2C+F%2E%22">Labombarda, F.</searchLink><relatesTo>4</relatesTo><br /><searchLink fieldCode="AR" term="%22Richard%2C+P%2E%22">Richard, P.</searchLink><relatesTo>5</relatesTo><br /><searchLink fieldCode="AR" term="%22Bonne%2C+G%2E%22">Bonne, G.</searchLink><relatesTo>6</relatesTo><br /><searchLink fieldCode="AR" term="%22Leturcq%2C+F%2E%22">Leturcq, F.</searchLink><relatesTo>7</relatesTo><br /><searchLink fieldCode="AR" term="%22Chapon%2C+F%2E%22">Chapon, F.</searchLink><relatesTo>4</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Neuromuscular+Disorders%22">Neuromuscular Disorders</searchLink>. Oct2014, Vol. 24 Issue 9/10, p843-844. 2p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=97955578 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.nmd.2014.06.172 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 2 StartPage: 843 Titles: – TitleFull: G.P.142: A new EMD gene missense mutation in exon 1 leads to absence of emerin and is responsible for X-linked dilated cardiomyopathy with conduction defects and arrhythmias and almost elusive skeletal muscle features. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Ben Yaou, R. – PersonEntity: Name: NameFull: Gerard, M. – PersonEntity: Name: NameFull: Chami, K. – PersonEntity: Name: NameFull: Sehier, A. – PersonEntity: Name: NameFull: Belin, A. – PersonEntity: Name: NameFull: Labombarda, F. – PersonEntity: Name: NameFull: Richard, P. – PersonEntity: Name: NameFull: Bonne, G. – PersonEntity: Name: NameFull: Leturcq, F. – PersonEntity: Name: NameFull: Chapon, F. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 10 Text: Oct2014 Type: published Y: 2014 Identifiers: – Type: issn-print Value: 09608966 Numbering: – Type: volume Value: 24 – Type: issue Value: 9/10 Titles: – TitleFull: Neuromuscular Disorders Type: main |
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