Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12. (Q44917198)

7 December 2017

Isolated left ventricular noncompaction is rarely caused by mutations in G4.5, alpha-dystrobrevin and FK Binding Protein-12. (English)

1 reference

left ventricular noncompaction

7 December 2017

1 reference

11

Jeffrey A Towbin

1 reference

7 December 2017

Alexander B Kenton

1

1 reference

7 December 2017

Ximena Sanchez

2

1 reference

7 December 2017

Karen J Coveler

3

1 reference

7 December 2017

Kimberly A Makar

4

1 reference

7 December 2017

Shinawe Jimenez

5

1 reference

7 December 2017

Fukiko Ichida

6

1 reference

7 December 2017

Ross T Murphy

7

1 reference

7 December 2017

Perry M Elliott

8

1 reference

7 December 2017

William McKenna

9

1 reference

7 December 2017

Neil E Bowles

10

1 reference

7 December 2017

Karla R Bowles

12

1 reference

7 December 2017

1 June 2004

1 reference

Molecular Genetics and Metabolism

7 December 2017

1 reference

7 December 2017

82

1 reference

7 December 2017

2

1 reference

7 December 2017

162-166

1 reference

Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy

7 December 2017

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Persisting myocardial sinusoids of both ventricles as an isolated anomaly: echocardiographic, angiographic, and pathologic anatomical findings

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Report of the 1995 World Health Organization/International Society and Federation of Cardiology Task Force on the Definition and Classification of cardiomyopathies.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Isolated noncompaction of left ventricular myocardium. A study of eight cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Xq28-linked noncompaction of the left ventricular myocardium: prenatal diagnosis and pathologic analysis of affected individuals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Mutation characterization and genotype-phenotype correlation in Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Infantile dilated X-linked cardiomyopathy, G4.5 mutations, altered lipids, and ultrastructural malformations of mitochondria in heart, liver, and skeletal muscle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Light at the end of the Ca(2+)-release channel tunnel: structures and mechanisms involved in ion translocation in ryanodine receptor channels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Detection of adenoviral genome in the myocardium of adult patients with idiopathic left ventricular dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Mutation analysis of the G4.5 gene in patients with isolated left ventricular noncompaction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

Isolated noncompaction of the left ventricular myocardium in the adult is an autosomal dominant disorder in the majority of patients

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.02.009

10.1016/J.YMGME.2004.02.009

7 January 2021

Identifiers

DOI

1 reference

7 December 2017

1 reference