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

7 December 2017

title

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

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left ventricular noncompaction

7 December 2017

main subject

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11

Jeffrey A Towbin

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7 December 2017

Alexander B Kenton

1

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7 December 2017

Ximena Sanchez

2

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7 December 2017

Karen J Coveler

3

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7 December 2017

Kimberly A Makar

4

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7 December 2017

Shinawe Jimenez

5

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7 December 2017

Fukiko Ichida

6

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7 December 2017

Ross T Murphy

7

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7 December 2017

Perry M Elliott

8

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7 December 2017

William McKenna

9

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7 December 2017

Neil E Bowles

10

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7 December 2017

Karla R Bowles

12

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7 December 2017

publication date

1 June 2004

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Molecular Genetics and Metabolism

7 December 2017

published in

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7 December 2017

volume

82

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7 December 2017

issue

2

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7 December 2017

page(s)

162-166

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

7 December 2017

cites work

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7 January 2021

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7 January 2021

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

7 January 2021

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Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

7 January 2021

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

7 January 2021

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Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

7 January 2021

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Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

7 January 2021

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

7 January 2021

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

7 January 2021

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Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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

7 January 2021

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7 January 2021

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10.1016/J.YMGME.2004.02.009

7 January 2021

Identifiers

DOI

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7 December 2017

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