Phospholipid Profiles Are Selectively Altered in the Putamen and White Frontal Cortex of Huntington’s Disease

Huntington’s disease (HD) is a genetic, neurodegenerative illness that onsets in late adulthood as a series of progressive and terminal cognitive, motor, and psychiatric deficits. The disease is caused by a polyQ mutation in the Huntingtin gene (HTT), producing a polyglutamine expansion in the Hunti...

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Detalles Bibliográficos
Autores principales: Phillips, Gabrielle R., Hancock, Sarah E., Jenner, Andrew M., McLean, Catriona, Newell, Kelly A., Mitchell, Todd W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143248/
https://www.ncbi.nlm.nih.gov/pubmed/35631226
http://dx.doi.org/10.3390/nu14102086

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143248/
https://www.ncbi.nlm.nih.gov/pubmed/35631226
http://dx.doi.org/10.3390/nu14102086

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