A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (Q72781923)

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29 October 2019

title

A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1 (English)

1 reference

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29 October 2019

main subject

dilated cardiomyopathy

1 reference

Kass S

1

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29 October 2019

MacRae C

2

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29 October 2019

Graber HL

3

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29 October 2019

Sparks EA

4

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29 October 2019

McNamara D

5

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29 October 2019

Boudoulas H

6

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29 October 2019

Basson CT

7

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29 October 2019

Baker PB 3rd

8

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29 October 2019

Cody RJ

9

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29 October 2019

Fishman MC

10

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29 October 2019

publication date

1 August 1994

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29 October 2019

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29 October 2019

volume

7

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29 October 2019

issue

4

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29 October 2019

page(s)

546-551

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https://scigraph.springernature.com/pub.10.1038/ng0894-546

29 October 2019

exact match

0 references

cites work

Epidemiology of idiopathic dilated and hypertrophic cardiomyopathy. A population-based study in Olmsted County, Minnesota, 1975-1984

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Prevalence and etiology of idiopathic dilated cardiomyopathy (summary of a National Heart, Lung, and Blood Institute workshop

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7 January 2021

The Frequency of Familial Dilated Cardiomyopathy in a Series of Patients with Idiopathic Dilated Cardiomyopathy

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X-linked dilated cardiomyopathy

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7 January 2021

Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathy.

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7 January 2021

Dystrophin analysis in idiopathic dilated cardiomyopathy

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7 January 2021

Cardiomyopathy in the Kearns-Sayre syndrome

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7 January 2021

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

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7 January 2021

Familial dilated cardiomyopathy

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7 January 2021

Hereditary progressive atrioventricular conduction defect. A new syndrome?

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7 January 2021

Clinical and pathologic study of familial dilated cardiomyopathy

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7 January 2021

Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3

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7 January 2021

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

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7 January 2021

Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11

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7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

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7 January 2021

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

1 reference

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7 January 2021

HLA class II (DR and DQ) antigen associations in idiopathic dilated cardiomyopathy. Validation study and meta-analysis of published HLA association studies

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7 January 2021

T-cell receptor gene polymorphisms in familial cardiomyopathy: correlation with anti-beta-receptor autoantibodies

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7 January 2021

A second-generation linkage map of the human genome

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https://api.crossref.org/works/10.1038%2FNG0894-546

7 January 2021

Integrated human genome-wide maps constructed using the CEPH reference panel.

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7 January 2021

A PCR-based linkage map of human chromosome 1.

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7 January 2021

Sequential imputation and multipoint linkage analysis

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7 January 2021

Connexin family of gap junction proteins

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7 January 2021

Gap junctions: new tools, new answers, new questions

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

Cardiac myocytes express multiple gap junction proteins

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https://api.crossref.org/works/10.1038%2FNG0894-546

7 January 2021

Distinct patterns of connexin expression in canine Purkinje fibers and ventricular muscle

1 reference

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7 January 2021

Reduced content of connexin43 gap junctions in ventricular myocardium from hypertrophied and ischemic human hearts

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-546

7 January 2021

Molecular cloning and functional expression of human connexin37, an endothelial cell gap junction protein

1 reference

https://api.crossref.org/works/10.1038%2FNG0894-546

7 January 2021

The quest for optimal electrocardiography. Tast Force I: standardization of terminology and interpretation

1 reference

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7 January 2021

Identifiers

DOI

10.1038/NG0894-546

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7951328%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference