Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide
Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide
About this item
Full title
Author / Creator
Publisher
New York: Springer US
Journal title
Language
English
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Publication information
Publisher
New York: Springer US
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Scope and Contents
Contents
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 BTHS patients is related primarily to progressive...
Alternative Titles
Full title
Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide
Authors, Artists and Contributors
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Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7895793
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7895793
Other Identifiers
ISSN
1382-4147
E-ISSN
1573-7322
DOI
10.1007/s10741-020-10031-3
