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Serum Raman spectroscopy as a diagnostic tool in patients with Huntington's disease
Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by an abnormal CAG expansion in exon 1 of the huntingtin (HTT) gene. Given its genetic basis it is possible to study patients both in the pre-manifest and manifest stages of the condition. While disease onset c...
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| Publicado no: | Chem Sci |
|---|---|
| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Royal Society of Chemistry
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7067270/ https://ncbi.nlm.nih.gov/pubmed/32190272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1039/c9sc03711j |
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