Mitochondrial dysfunctions in barth syndrome-Reference-Cited by-同舟云学术

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Mitochondrial dysfunctions in barth syndrome

Published:2019-02-11 Issue:7 Volume:71 Page:791-801
ISSN:1521-6543
Container-title:IUBMB Life
language:en
Short-container-title:IUBMB Life

Author:

Ghosh Sagnika¹,Iadarola Donna M.¹,Ball Writoban Basu¹,Gohil Vishal M.¹^ORCID

Affiliation:

1. Department of Biochemistry and Biophysics; Texas A&M University; College Station TX USA

Funder

National Institute of General Medical Sciences

National Institutes of Health

Welch Foundation

Publisher

Wiley

Subject

Cell Biology,Clinical Biochemistry,Genetics,Molecular Biology,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/iub.2018/fullpdf

Reference71 articles.

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

2. Barth syndrome;Clarke;Orphanet J. Rare Dis.,2013

3. A novel X-linked gene, G4.5. Is responsible for Barth syndrome;Bione;Nat. Genet.,1996

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

5. Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome;Schlame;Ann. Neurol.,2002

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1. The subtherapeutic dose of valproic acid induces the activity of cardiolipin-dependent proteins;Biochimica et Biophysica Acta (BBA) - Bioenergetics;2024-11

2. The metabolic basis of inherited neutropenias;British Journal of Haematology;2023-12-04

3. Cardiolipin deficiency leads to the destabilization of mitochondrial magnesium channel MRS2 in Barth syndrome;Human Molecular Genetics;2023-09-18

4. Mitochondrial phospholipid metabolism in health and disease;Journal of Cell Science;2023-09-01

5. Case report: Variability in clinical features as a potential pitfall for the diagnosis of Barth syndrome;Frontiers in Pediatrics;2023-08-16

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