Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome-Reference-Cited by-同舟云学术

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Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome

Published:2015-12 Issue: Volume:193 Page:1-10
ISSN:0009-3084
Container-title:Chemistry and Physics of Lipids
language:en
Short-container-title:Chemistry and Physics of Lipids

Author:

Gaspard Gerard J.,McMaster Christopher R.

Funder

Barth Syndrome Foundation of Canada

Genome Canada

Genome Atlantic

Nova Scotia Research and Innovation Trust

Dalhousie Medical Research Foundation

Publisher

Elsevier BV

Subject

Cell Biology,Organic Chemistry,Molecular Biology,Biochemistry

Reference130 articles.

1. Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography;Acehan;Lab. Invest.,2007

2. Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria;Acehan;Mitochondrion,2009

3. Cardiolipin affects the supramolecular organization of ATP synthase in mitochondria;Acehan;Biophys. J.,2011

4. Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome;Acehan;J. Biol. Chem.,2011

5. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28;Ades;Am. J. Med. Genet.,1993

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