Investigating the Transition of Pre-Symptomatic to Symptomatic Huntington’s Disease Status Based on Omics Data

Huntington’s disease is a rare neurodegenerative disease caused by a cytosine–adenine–guanine (CAG) trinucleotide expansion in the Huntingtin (HTT) gene. Although Huntington’s disease (HD) is well studied, the pathophysiological mechanisms, genes and metabolites involved in HD remain poorly understo...

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Detalles Bibliográficos
Autores principales: Christodoulou, Christiana C., Zachariou, Margarita, Tomazou, Marios, Karatzas, Evangelos, Demetriou, Christiana A., Zamba-Papanicolaou, Eleni, Spyrou, George M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582902/
https://www.ncbi.nlm.nih.gov/pubmed/33049985
http://dx.doi.org/10.3390/ijms21197414

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582902/
https://www.ncbi.nlm.nih.gov/pubmed/33049985
http://dx.doi.org/10.3390/ijms21197414

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