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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Detalles Bibliográficos
Autores principales: Wilson, Lori D, Al-Majid, Sadeeka, Rakovski, Cyril S, MD, Christina D Schwindt
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414836/
https://www.ncbi.nlm.nih.gov/pubmed/22721508
http://dx.doi.org/10.1186/1476-9255-9-25

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414836/
https://www.ncbi.nlm.nih.gov/pubmed/22721508
http://dx.doi.org/10.1186/1476-9255-9-25

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