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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Detalles Bibliográficos
Autores principales: Huefner, Anna, Kuan, Wei-Li, Mason, Sarah L., Mahajan, Sumeet, Barker, Roger A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067270/
https://www.ncbi.nlm.nih.gov/pubmed/32190272
http://dx.doi.org/10.1039/c9sc03711j

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7067270/
https://www.ncbi.nlm.nih.gov/pubmed/32190272
http://dx.doi.org/10.1039/c9sc03711j

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