Interplay between cardiolipin and plasmalogens in Barth syndrome
Author:
Affiliation:
1. Department of Biochemistry and Biomedical Sciences McMaster University, Health Sciences Centre Hamilton Ontario Canada
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12449
Reference84 articles.
1. Inflammation and metabolic disorders
2. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): Respiratory-chain abnormalities in cultured fibroblasts
3. A novel X-linked gene, G4.5. is responsible for Barth syndrome
4. Phospholipid abnormalities in children with Barth syndrome
5. Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome
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