A rare form of LIM domain-binding protein 3 (LDB3) mutation causes hypertrophic cardiomyopathy and myofibrillar myopathy type 4.
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| Title: | A rare form of LIM domain-binding protein 3 (LDB3) mutation causes hypertrophic cardiomyopathy and myofibrillar myopathy type 4. |
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| Authors: | Svaguša T; Department of Cardiovascular Diseases, Dubrava University Hospital, Zagreb, Croatia., Sedlić F; Department of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia., Županić S; Department of Neurology, Dubrava University Hospital, Zagreb, Croatia., Manola Š; Department of Cardiovascular Diseases, Dubrava University Hospital, Zagreb, Croatia., Bakoš M; Department of Pediatrics, University Hospital Centre Zagreb, Zagreb, Croatia., Mirošević V; Department of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia., Livun A; Department of Scientific Research and Translational Medicine, Dubrava University Hospital, Zagreb, Croatia. |
| Source: | Clinical genetics [Clin Genet] 2024 Nov; Vol. 106 (5), pp. 659-660. Date of Electronic Publication: 2024 Jul 11. |
| Publication Type: | Case Reports; Letter; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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| FullText | Links: – Type: pdflink Text: Availability: 1 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 38992921 AccessLevel: 2 PubType: Report PubTypeId: report PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: A rare form of LIM domain-binding protein 3 (LDB3) mutation causes hypertrophic cardiomyopathy and myofibrillar myopathy type 4. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Svaguša+T%22">Svaguša T</searchLink>; Department of Cardiovascular Diseases, Dubrava University Hospital, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Sedlić+F%22">Sedlić F</searchLink>; Department of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Županić+S%22">Županić S</searchLink>; Department of Neurology, Dubrava University Hospital, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Manola+Š%22">Manola Š</searchLink>; Department of Cardiovascular Diseases, Dubrava University Hospital, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Bakoš+M%22">Bakoš M</searchLink>; Department of Pediatrics, University Hospital Centre Zagreb, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Mirošević+V%22">Mirošević V</searchLink>; Department of Pathophysiology, University of Zagreb School of Medicine, Zagreb, Croatia.<br /><searchLink fieldCode="AU" term="%22Livun+A%22">Livun A</searchLink>; Department of Scientific Research and Translational Medicine, Dubrava University Hospital, Zagreb, Croatia. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2024 Nov; Vol. 106 (5), pp. 659-660. <i>Date of Electronic Publication: </i>2024 Jul 11. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Letter; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=38992921 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.14585 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 659 Titles: – TitleFull: A rare form of LIM domain-binding protein 3 (LDB3) mutation causes hypertrophic cardiomyopathy and myofibrillar myopathy type 4. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Svaguša T – PersonEntity: Name: NameFull: Sedlić F – PersonEntity: Name: NameFull: Županić S – PersonEntity: Name: NameFull: Manola Š – PersonEntity: Name: NameFull: Bakoš M – PersonEntity: Name: NameFull: Mirošević V – PersonEntity: Name: NameFull: Livun A IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 11 Text: 2024 Nov Type: published Y: 2024 Identifiers: – Type: issn-electronic Value: 1399-0004 Numbering: – Type: volume Value: 106 – Type: issue Value: 5 Titles: – TitleFull: Clinical genetics Type: main |
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