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Clinical utility of serum biomarkers in Duchenne muscular dystrophy

Assessments of disease progression and response to therapies in Duchenne muscular dystrophy (DMD) patients remain challenging. Current DMD patient assessments include complex physical tests and invasive procedures such as muscle biopsies, which are not suitable for young children. Defining alternati...

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Detalhes bibliográficos
Publicado no:Clin Proteomics
Main Authors: Hathout, Yetrib, Seol, Haeri, Han, Meng Hsuan J., Zhang, Aiping, Brown, Kristy J., Hoffman, Eric P.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4820909/
https://ncbi.nlm.nih.gov/pubmed/27051355
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12014-016-9109-x
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