Pathogenesis of Huntington’s Disease: An Emphasis on Molecular Pathways and Prevention by Natural Remedies

Background: Huntington’s disease is an inherited autosomal dominant trait neuro-degenerative disorder caused by changes (mutations) of a gene called huntingtin (htt) that is located on the short arm (p) of chromosome 4, CAG expansion mutation. It is characterized by unusual movements, cognitive and...

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Detalles Bibliográficos
Autores principales: Irfan, Zainab, Khanam, Sofia, Karmakar, Varnita, Firdous, Sayeed Mohammed, El Khier, Bothaina Samih Ismail Abou, Khan, Ilyas, Rehman, Muneeb U., Khan, Andleeb
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599635/
https://www.ncbi.nlm.nih.gov/pubmed/36291322
http://dx.doi.org/10.3390/brainsci12101389

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599635/
https://www.ncbi.nlm.nih.gov/pubmed/36291322
http://dx.doi.org/10.3390/brainsci12101389

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