(Q35249710)

7 August 2017

title

Linkage of Familial Dilated Cardiomyopathy with Conduction Defect and Muscular Dystrophy to Chromosome 6q23 (English)

1 reference

26 November 2024

main subject

dilated cardiomyopathy

1 reference

familial dilated cardiomyopathy

inferred from title

1 reference

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

26 November 2024

genetic linkage

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

Margaret A. Pericak-Vance

26 November 2024

author

3

object named as

M A Pericak-Vance

1 reference

7 August 2017

4

E. M. McNally

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

26 November 2024

author name string

D. N. Messina

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

26 November 2024

M. C. Speer

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

26 November 2024

language of work or name

English

0 references

publication date

1 October 1997

1 reference

7 August 2017

October 1997

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9382102

full work available at URL

26 November 2024

https://doi.org/10.1086/514896

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

https://europepmc.org/articles/PMC1715999

26 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

https://europepmc.org/articles/PMC1715999?pdf=render

26 November 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A9382102

https://api.elsevier.com/content/article/PII:S0002929707641998?httpAccept=text/xml

26 November 2024

1 reference

https://api.elsevier.com/content/article/PII:S0002929707641998?httpAccept=text/plain

26 November 2024

1 reference

American Journal of Human Genetics

26 November 2024

published in

1 reference

7 August 2017

volume

61

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7 August 2017

issue

4

1 reference

7 August 2017

page(s)

909-917

1 reference

Dystrophia Muscularis: A HEREDITARY PRIMARY MYOPATHY IN THE HOUSE MOUSE.

7 August 2017

cites work

1 reference

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Genetic localization of a newly recognized autosomal dominant limb-girdle muscular dystrophy with cardiac involvement (LGMD1B) to chromosome 1q11-21.

12 July 2018

1 reference

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Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy

12 July 2018

1 reference

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Merosin/laminin-2 and muscular dystrophy

12 July 2018

1 reference

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Beyond dystrophin: current progress in the muscular dystrophies

12 July 2018

1 reference

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A Gene Map of the Human Genome

12 July 2018

1 reference

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Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23.

12 July 2018

1 reference

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Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin alpha2-chain in congenital muscular dystrophy with partial deficiency of the protein.

12 July 2018

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A collection of tri- and tetranucleotide repeat markers used to generate high quality, high resolution human genome-wide linkage maps

12 July 2018

1 reference

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Mapping a cardiomyopathy locus to chromosome 3p22-p25.

12 July 2018

1 reference

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Familial hypertrophic cardiomyopathy: a genetic model of cardiac hypertrophy

12 July 2018

1 reference

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Dystrophin-associated proteins in muscular dystrophy

12 July 2018

1 reference

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Localization of a gene responsible for familial dilated cardiomyopathy to chromosome 1q32.

12 July 2018

1 reference

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Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage.

12 July 2018

1 reference

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Linkage of familial dilated cardiomyopathy to chromosome 9. Heart Muscle Disease Study Group.

12 July 2018

1 reference

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Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

12 July 2018

1 reference

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Strategies for multilocus linkage analysis in humans

12 July 2018

1 reference

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Muscular dystrophy in the mouse caused by an allele at the dy-locus

12 July 2018

1 reference

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Familial automaticity-conduction disorder with associated cardiomyopathy.

12 July 2018

1 reference

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A simple salting out procedure for extracting DNA from human nucleated cells

12 July 2018

1 reference

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

12 July 2018

1 reference

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Confirmation of genetic heterogeneity in limb-girdle muscular dystrophy: linkage of an autosomal dominant form to chromosome 5q

12 July 2018

1 reference

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

12 July 2018

1 reference

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Idiopathic Dilated Cardiomyopathy

26 September 2018

1 reference

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

8 December 2018

1 reference

12 December 2020

Deficiency of merosin (laminin M or alpha 2) in congenital muscular dystrophy associated with cerebral white matter alterations

1 reference

12 December 2020

X-linked dilated cardiomyopathy

1 reference

12 December 2020

Inherited cardiomyopathies

1 reference

12 December 2020

A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement

1 reference

12 December 2020

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome maps 7. The human transcript map. Wall chart

26

1 reference

26 November 2024

Identifiers

DOI

10.1086/514896

1 reference

7 August 2017

1 reference

7 August 2017

1 reference