Increased systemic HSP70B levels in spinal muscular atrophy infants

Despite newly available treatments for spinal muscular atrophy (SMA), novel circulating biomarkers are still critically necessary to track SMA progression and therapeutic response. To identify potential biomarkers, we performed whole‐blood RNA sequencing analysis in SMA type 1 subjects under 1 year...

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Detalhes bibliográficos
Publicado no:Ann Clin Transl Neurol
Main Authors: Eichelberger, Eric J., Alves, Christiano R. R., Zhang, Ren, Petrillo, Marco, Cullen, Patrick, Farwell, Wildon, Hurt, Jessica A., Staropoli, John F., Swoboda, Kathryn J.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2021
Assuntos:
Brief Communications
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8283166/
https://ncbi.nlm.nih.gov/pubmed/33991176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.51377
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