A Glimpse of Molecular Biomarkers in Huntington’s Disease

Huntington’s disease (HD) is a devastating neurodegenerative disorder that is caused by an abnormal expansion of CAG repeats in the Huntingtin (HTT) gene. Although the main symptomatology is explained by alterations at the level of the central nervous system, predominantly affecting the basal gangli...

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Detalles Bibliográficos
Autores principales: Martí-Martínez, Silvia, Valor, Luis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142992/
https://www.ncbi.nlm.nih.gov/pubmed/35628221
http://dx.doi.org/10.3390/ijms23105411

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9142992/
https://www.ncbi.nlm.nih.gov/pubmed/35628221
http://dx.doi.org/10.3390/ijms23105411

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