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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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| Vydáno v: | Heart Fail Rev |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Springer US
2020
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| Témata: | |
| On-line přístup: | 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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