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Higher IL-6 and IL6:IGF Ratio in Patients with Barth Syndrome
BACKGROUND: Barth Syndrome (BTHS) is a serious X-linked genetic disorder associated with mutations in the tafazzin gene (TAZ, also called G4.5). The multi-system disorder is primarily characterized by the following pathologies: cardiac and skeletal myopathies, neutropenia, growth delay, and exercise...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3414836/ https://ncbi.nlm.nih.gov/pubmed/22721508 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1476-9255-9-25 |
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