Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography-Reference-Cited by-同舟云学术

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Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography

Published:2006-10-16 Issue:1 Volume:87 Page:40-48
ISSN:0023-6837
Container-title:Laboratory Investigation
language:en
Short-container-title:Lab Invest

Author:

Acehan Devrim,Xu Yang,Stokes David L,Schlame Michael

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology,Molecular Biology,Pathology and Forensic Medicine

Link

http://www.nature.com/articles/3700480.pdf

Reference42 articles.

1. Barth PG, Scholte HR, Berden JA, et al. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leukocytes. J Neurol Sci 1983;62:327–355.

2. Kelley RI, Cheatham JP, Clark BJ, et al. X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria. J Pediatr 1991;119:738–747.

3. Barth PG, Wanders RJA, Vreken P, et al. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060). J Inher Metab Dis 1999;22:555–567.

4. Bione S, D'Adamo P, Maestrini E, et al. A novel X-linked gene, G4.5, is responsible for Barth syndrome. Nat Genet 1996;12:385–389.

5. Ma L, Vaz FM, Gu Z, et al. The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Δ mutant. Implications for Barth syndrome. J Biol Chem 2004;279:44394–44399.

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