Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy (Q44163813)

30 November 2017

title

Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy (English)

1 reference

30 November 2017

4

Jeffrey A Towbin

1 reference

30 November 2017

Jinong Feng

1

1 reference

30 November 2017

Jin Yan

series ordinal

2

1 reference

30 November 2017

Carolyn H Buzin

series ordinal

3

1 reference

30 November 2017

Steve S Sommer

series ordinal

5

1 reference

30 November 2017

publication date

1 September 2002

1 reference

Molecular Genetics and Metabolism

30 November 2017

published in

1 reference

30 November 2017

volume

77

1 reference

30 November 2017

issue

1-2

1 reference

30 November 2017

page(s)

119-126

1 reference

The "final common pathway" hypothesis and inherited cardiovascular disease. The role of cytoskeletal proteins in dilated cardiomyopathy

30 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Cardiac function in Duchenne's muscular dystrophy. Results of 10-year follow-up study and noninvasive tests

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

The cardiomyopathy of progressive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

A mutation in the dystrophin gene selectively affecting dystrophin expression in the heart

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Dystrophin gene abnormalities in two patients with idiopathic dilated cardiomyopathy.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Prevalence and characteristics of dystrophin defects in adult male patients with dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Diagnosis of Duchenne dystrophy by enhanced detection of small mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Scanning by DOVAM-S detects all unique sequence changes in blinded analyses: evidence that the scanning conditions are generic

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Detection of virtually all mutations-SSCP (DOVAM-S): a rapid method for mutation scanning with virtually 100% sensitivity

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Germline origins in the human F9 gene: frequent G:C-->A:T mosaicism and increased mutations with advanced maternal age.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Dystrophin and utrophin: the missing links!

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Somatic mosaicism and female-to-female transmission in a kindred with hemophilia B (factor IX deficiency).

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Enteroviral protease 2A directly cleaves dystrophin and is inhibited by a dystrophin-based substrate analogue

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Suggestions concerning the relationship between mutant frequency and mutation rate at the hprt locus in human peripheral T-lymphocytes.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Single base-pair substitutions in pathology and evolution: Two sides to the same coin

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

VAPSE-based analysis: a two-phased candidate gene approach for elucidating genetic predisposition to complex disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

Clustering of missense mutations in the ataxia-telanglectasia gene in a sporadic T-cell leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

ATM mutations and phenotypes in ataxia-telangiectasia families in the British Isles: expression of mutant ATM and the risk of leukemia, lymphoma, and breast cancer

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2802%2900153-1

7 January 2021

10.1016/S1096-7192(02)00153-1

Identifiers

DOI

1 reference

30 November 2017

1 reference