A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1-Reference-Cited by-同舟云学术

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A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1

Published:2005-10-14 Issue:3-4 Volume:118 Page:451-457
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Schönberger Jost,Kühler Leif,Martins Elisabete,Lindner Tom H.,Silva-Cardoso Jose,Zimmer Michael

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-005-0064-2.pdf

Reference37 articles.

1. Abecasis GR, Cherny SS, Cookson WO, Cardon LR (2002) Merlin–rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 30:97–101

2. Bione S, D’Adamo P, Maestrini E, Gedeon AK, Bolhuis PA, Toniolo D (1996) A novel X-linked gene, G4.5. is responsible for Barth syndrome. Nat Genet 12:385–389

3. Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, Roberts R, Pignatelli R, Towbin JA (1996) Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21–23. J Clin Invest 98:1355–1360

4. Bowles NE, Bowles KR, Towbin JA (2000) The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy. Herz 25:168–175

5. Braunwald E (1997) Shattuck lecture–cardiovascular medicine at the turn of the millennium: triumphs, concerns, and opportunities. N Engl J Med 337:1360–1369

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1. Proteomic Analysis of Atrial Appendages Revealed the Pathophysiological Changes of Atrial Fibrillation;Frontiers in Physiology;2020-09-16

2. Molecular characterization of Portuguese patients with dilated cardiomyopathy;Revista Portuguesa de Cardiologia;2019-02

3. Molecular characterization of Portuguese patients with dilated cardiomyopathy;Revista Portuguesa de Cardiologia (English Edition);2019-02

4. Genome-Wide Linkage Analysis of Cardiovascular Disease Biomarkers in a Large, Multigenerational Family;PLoS ONE;2013-08-02

5. Rare variant mutations identified in pediatric patients with dilated cardiomyopathy;Progress in Pediatric Cardiology;2011-01

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