Barth syndrome in a female patient-Reference-Cited by-同舟云学术

Barth syndrome in a female patient

Published:2012-05 Issue:1 Volume:106 Page:115-120
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Cosson Laure,Toutain Annick,Simard Gilles,Kulik Willem,Matyas Gabor,Guichet Agnès,Blasco Hélène,Maakaroun-Vermesse Zoha,Vaillant Marie-Catherine,Le Caignec Cédric,Chantepie Alain,Labarthe François

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference21 articles.

1. An X-linkedmitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J. Neurol. Sci.,1983

2. Xlinked cardioskeletal myopathy and neutropenia (Barth syndrome): an update;Barth;Am. J. Med. Genet. A,2004

3. Cardiac and clinical phenotype in Barth syndrome;Spencer;Pediatrics,2006

4. The enzymatic function of tafazzin;Xu;J. Biol. Chem.,2006

5. The enigmatic role of tafazzin in cardiolipin metabolism;Houtkooper;Biochim. Biophys. Acta,2009

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