(Q34027566)

30 July 2017

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title

Genetic abnormalities responsible for dilated cardiomyopathy (English)

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30 July 2017

main subject

dilated cardiomyopathy

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Towbin JA

1

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30 July 2017

Bowles NE

series ordinal

2

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30 July 2017

publication date

1 September 2000

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Current cardiology reports

30 July 2017

published in

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30 July 2017

volume

2

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30 July 2017

issue

5

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30 July 2017

page(s)

475-480

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https://scigraph.springernature.com/pub.10.1007/s11886-000-0063-9

30 July 2017

exact match

0 references

cites work

Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0063-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0063-9

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0063-9

Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11886-000-0063-9

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

21 January 2018

1 reference

12 December 2020

X-linked muscular dystrophy with early contractures and cardiomyopathy (Emery-Dreifuss type).

1 reference

12 December 2020

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

1 reference

12 December 2020

Dystrophies and heart disease.

1 reference

12 December 2020

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

12 December 2020

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria

1 reference

12 December 2020

Insertional mutation by transposable element, L1, in the DMD gene results in X-linked dilated cardiomyopathy

1 reference

12 December 2020

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

1 reference

12 December 2020

A novel X-linked gene, G4.5. is responsible for Barth syndrome

1 reference

12 December 2020

Complete cloning of the duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals

1 reference

12 December 2020

Infantile dilated cardiomyopathy. Relation of outcome to left ventricular mechanics, hemodynamics, and histology at the time of presentation

1 reference

12 December 2020

Prognostic features of children with idiopathic dilated cardiomyopathy

1 reference

12 December 2020

Frequency and phenotypes of familial dilated cardiomyopathy.

1 reference

12 December 2020

A novel Alu-like element rearranged in the dystrophin gene causes a splicing mutation in a family with X-linked dilated cardiomyopathy.

1 reference

12 December 2020

Genetics of neonatal cardiomyopathy

1 reference

12 December 2020

An X-linked recessive cardiomyopathy with abnormal mitochondria

1 reference

12 December 2020

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Etiologies of cardiomyopathy and heart failure

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy

1 reference

12 December 2020

X-linked dilated cardiomyopathy

1 reference

12 December 2020

Molecular genetic aspects of cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

12 December 2020

Inherited cardiomyopathies

1 reference

12 December 2020

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

1 reference

12 December 2020

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

1 reference

12 December 2020

Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23.

1 reference

12 December 2020

A Point Mutation in the 5' Splice Site of the Dystrophin Gene First Intron Responsible for X-Linked Dilated Cardiomyopathy

1 reference

12 December 2020

Clinical course of idiopathic dilated cardiomyopathy in children

1 reference

12 December 2020

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy

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

Mutation characterization and genotype-phenotype correlation in Barth syndrome

1 reference

12 December 2020

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

1 reference

12 December 2020

X-linked dilated cardiomyopathy. Novel mutation of the dystrophin gene

1 reference

12 December 2020

Familial dilated cardiomyopathy in the United Kingdom

1 reference

12 December 2020

Towards an understanding of the dystrophin-glycoprotein complex: linkage between the extracellular matrix and the membrane cytoskeleton in muscle fibers.

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

Uncommon myocardial diseases; the non-coronary cardiomyopathies

1 reference

12 December 2020

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

1 reference

12 December 2020

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

1 reference

12 December 2020

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

1 reference

12 December 2020

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.

1 reference

12 December 2020

10.1007/S11886-000-0063-9

Identifiers

DOI

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Dimensions Publication ID

30 July 2017

1032114127

0 references

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