Cardiac‐specific succinate dehydrogenase deficiency in Barth syndrome-Reference-Cited by-同舟云学术

Cardiac‐specific succinate dehydrogenase deficiency in Barth syndrome

Published:2015-12-23 Issue:2 Volume:8 Page:139-154
ISSN:1757-4676
Container-title:EMBO Molecular Medicine
language:en
Short-container-title:EMBO Mol Med

Author:

Dudek Jan¹,Cheng I‐Fen¹²,Chowdhury Arpita¹,Wozny Katharina³,Balleininger Martina¹,Reinhold Robert¹,Grunau Silke¹,Callegari Sylvie¹,Toischer Karl²⁴,Wanders Ronald JA⁵,Hasenfuß Gerd²⁴⁶,Brügger Britta³,Guan Kaomei²⁴⁶,Rehling Peter¹⁶⁷

Affiliation:

1. Department of Cellular Biochemistry University Medical Center Göttingen Göttingen Germany

2. Department of Cardiology and Pneumology University Medical Center Göttingen Göttingen Germany

3. Heidelberg University Biochemistry Center University Heidelberg Heidelberg Germany

4. German Center for Cardiovascular Research (DZHK) Göttingen Germany

5. Departments of Clinical Chemistry and Pediatrics Academic Medical Center University of Amsterdam Amsterdam The Netherlands

6. Heart Research Center Göttingen Göttingen Germany

7. Max Planck Institute for Biophysical Chemistry Göttingen Germany

Publisher

EMBO

Subject

Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/emmm.201505644

Reference53 articles.

1. Cardiac and Skeletal Muscle Defects in a Mouse Model of Human Barth Syndrome

2. Respiratory Active Mitochondrial Supercomplexes

3. Arrangement of electron transport chain components in bovine mitochondrial supercomplex I1III2IV1

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

5. Cardiolipin-dependent Reconstitution of Respiratory Supercomplexes from Purified Saccharomyces cerevisiae Complexes III and IV

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