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Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide

Barth syndrome (BTHS) is a rare, X-linked recessive, infantile-onset debilitating disorder characterized by early-onset cardiomyopathy, skeletal muscle myopathy, growth delay, and neutropenia, with a worldwide incidence of 1/300,000–400,000 live births. The high mortality rate throughout infancy in...

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Bibliografische gegevens
Gepubliceerd in:Heart Fail Rev
Hoofdauteur: Sabbah, Hani N.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Springer US 2020
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7895793/
https://ncbi.nlm.nih.gov/pubmed/33001359
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10741-020-10031-3
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