Huntingtin and the Synapse

Huntington disease (HD) is a monogenic disease that results in a combination of motor, psychiatric and cognitive symptoms. HD is caused by a CAG trinucleotide repeat expansion in the huntingtin (HTT) gene, which results in the production of a pathogenic mutant HTT protein (mHTT). Although there is n...

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Detalles Bibliográficos
Autores principales: Barron, Jessica C., Hurley, Emily P., Parsons, Matthew P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239291/
https://www.ncbi.nlm.nih.gov/pubmed/34211373
http://dx.doi.org/10.3389/fncel.2021.689332

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8239291/
https://www.ncbi.nlm.nih.gov/pubmed/34211373
http://dx.doi.org/10.3389/fncel.2021.689332

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