About: A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1

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About: A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 1994

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 1994 (uk) article scientifique publié en 1994 (fr) im August 1994 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'agostu de 1994 (ast) scientific article published on 01 August 1994 (en)
publication date	wds:Q72781923-B94A0CE3-13BA-40F3-9288-141EE69974E2
publication date	1994-08-01 00:00:00Z (xsd:dateTime)
exact match	wds:Q72781923-1D199FC7-45EF-415C-BBD1-0E26A9416505
exact match	https://scigraph.springernature.com/pub.10.1038/ng0894-546
cites work	wds:Q72781923-1D1BA892-4B0D-4868-949D-963C48EE8C2A wds:Q72781923-2D33F292-D842-4760-B9AB-C0070FE79EC4 wds:Q72781923-3006726D-D323-4191-8396-816E493AA6BF wds:Q72781923-3B08402B-69FC-429A-892B-A79F6DB88547 wds:Q72781923-41B64484-BABB-4B9A-98AD-29B7706C866C wds:Q72781923-45B2FEE2-91B2-4226-A77B-7589BF463DBA wds:Q72781923-53E25733-D921-4001-B0A5-7CD51A72487D wds:Q72781923-5ED3CDBA-7718-4E6C-AADC-A5510978E009 wds:Q72781923-682C54A2-85B6-4464-8921-029731F8CD8D wds:Q72781923-69514D59-1771-4DE9-A754-C9BF2D128EA8 wds:Q72781923-743E6A38-8B68-48D8-873D-06AE8C4D68F6 wds:Q72781923-76294905-674D-4CB1-8C81-D2F25445C5B0 wds:Q72781923-7F291415-B24C-42DE-9435-A45915961E16 wds:Q72781923-803DC33E-2CFC-4512-B816-422692EB0ABB wds:Q72781923-813F3455-4264-4511-91FD-983A69AC206D wds:Q72781923-9AB79CF0-BD19-4A60-8A14-3A6B15433C58 wds:Q72781923-9E905895-B2CB-4203-99E4-0840BF97A806 wds:Q72781923-ABAD8E16-D129-42F1-A3C2-D8AC21428204 wds:Q72781923-ADAB16AD-82FD-445E-B08D-E06946D3A33A wds:Q72781923-AEECCAF7-934C-4C0A-BFFC-7C57BF5CB6D2 wds:Q72781923-B9EBD591-A39F-4930-B1B4-3B6EC6A7C5AF wds:Q72781923-BC48AD2A-DDB9-4C2E-9E84-C2FEE44A7324 wds:Q72781923-C2C06768-B9F5-40FF-8923-E5253C6FD443 wds:Q72781923-D4D7F3D9-00F0-4925-AE97-9E689C1DCB26 wds:Q72781923-D75595B2-B502-4961-ACB5-A5E4B47F701C wds:Q72781923-DB64E499-9EDE-40C2-8EC5-E63F9F155C9C wds:Q72781923-E271D3D0-418A-4050-AF79-D73D85E1C763 wds:Q72781923-EADD33C1-70D7-4AE4-81A6-FE6DF29F77E4 wds:Q72781923-EE5E28BC-0CB2-46F4-956F-AD3EA199A885 wds:Q72781923-FD02F611-C6EA-43C5-80B7-521406F1958E
cites work	A second-generation linkage map of the human genome Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11 A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy Dystrophin analysis in idiopathic dilated cardiomyopathy The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy Integrated human genome-wide maps constructed using the CEPH reference panel. Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy. Connexin family of gap junction proteins Gap junctions: new tools, new answers, new questions Strategies for multilocus linkage analysis in humans Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984 Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop Hereditary progressive atrioventricular conduction defect. A new syndrome? Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3. Cardiac myocytes express multiple gap junction proteins Reduced content of connexin43 gap junctions in ventricular myocardium from hypertrophied and ischemic human hearts HLA class II (DR and DQ) antigen associations in idiopathic dilated cardiomyopathy. Validation study and meta-analysis of published HLA association studies Clinical and pathologic study of familial dilated cardiomyopathy T-cell receptor gene polymorphisms in familial cardiomyopathy: correlation with anti-beta-receptor autoantibodies X-linked dilated cardiomyopathy Sequential imputation and multipoint linkage analysis Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected A PCR-based linkage map of human chromosome 1. Distinct patterns of connexin expression in canine Purkinje fibers and ventricular muscle The quest for optimal electrocardiography. Tast Force I: standardization of terminology and interpretation Familial dilated cardiomyopathy Cardiomyopathy in the Kearns-Sayre syndrome Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3
author name string	wds:Q72781923-6019C783-9E72-43DD-9CEF-3F4FB37DBAC4 wds:Q72781923-695C66EC-E930-4425-B5EB-05526E0B84C7 wds:Q72781923-8E3AB5A3-BFD5-43B0-8C90-456F3099263D wds:Q72781923-9616701B-449C-4F20-9408-E4915AF00BAF wds:Q72781923-A358411F-2F7E-43ED-8080-3A17AC82ED5B wds:Q72781923-A98B8B18-0109-49A5-AFAD-64534B496DBC wds:Q72781923-B6246AA3-0424-4384-8B78-6E73BE6ACFA1 wds:Q72781923-CA7BD845-FBA6-4D60-BFCB-B848C4CDE183 wds:Q72781923-D9D493DF-8D44-45C2-B939-4E8DA25E85B9 wds:Q72781923-F9D9637A-D275-4C27-AE14-491271B36A0D
author name string	Fishman MC Boudoulas H McNamara D Basson CT Kass S Cody RJ MacRae C Baker PB 3rd Graber HL Sparks EA
rdfs:label	A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (en) A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (nl)
skos:prefLabel	A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (en) A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (nl)
name	A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (en) A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (nl)
title	wds:Q72781923-27DB2A29-43BC-4587-9DF8-EECA99C2CE93
title	A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (en)
page(s)	wds:Q72781923-84349B19-397F-4D1A-B53E-78368B2DC3B8

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