Infantile Dilated X-Linked Cardiomyopathy, G4.5 Mutations, Altered Lipids, and Ultrastructural Malformations of Mitochondria in Heart, Liver, and Skeletal Muscle

This publication has 21 references indexed in Scilit:

• Defective Remodeling of Cardiolipin and Phosphatidylglycerol in Barth Syndrome
  Biochemical and Biophysical Research Communications, 2000
• Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
  American Journal of Human Genetics, 1997
• The X-Linked Gene G4.5 Is Responsible for Different Infantile Dilated Cardiomyopathies
  American Journal of Human Genetics, 1997
• Neonatal, Lethal Noncompaction of the Left Ventricular Myocardium Is Allelic with Barth Syndrome
  American Journal of Human Genetics, 1997
• A novel X-linked gene, G4.5. is responsible for Barth syndrome
  Nature Genetics, 1996
• X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory‐chain abnormalities in cultured fibroblasts
  Journal of Inherited Metabolic Disease, 1996
• Dilated cardiomyopathy due to type II X-linked 3-methylglutaconic aciduria: successful treatment with pantothenic acid.
  Heart, 1994
• Hemodynamic and myocyte mitochondrial ultrastructural abnormalities in arrhythmogenic right ventricular dysplasia
  American Heart Journal, 1993
• Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene.
  Genome Research, 1992
• X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria
  The Journal of Pediatrics, 1991