Huntington disease: Advances in the understanding of its mechanisms()

Huntington disease (HD) is a devastating monogenic autosomal dominant disorder. HD is caused by a CAG expansion in exon 1 of the gene coding for huntingtin, placed in the short arm of chromosome 4. Despite its well-defined genetic origin, the molecular and cellular mechanisms underlying the disease...

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Detalles Bibliográficos
Autores principales: Gatto, Emilia M., Rojas, Natalia González, Persi, Gabriel, Etcheverry, José Luis, Cesarini, Martín Emiliano, Perandones, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298812/
https://www.ncbi.nlm.nih.gov/pubmed/34316639
http://dx.doi.org/10.1016/j.prdoa.2020.100056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8298812/
https://www.ncbi.nlm.nih.gov/pubmed/34316639
http://dx.doi.org/10.1016/j.prdoa.2020.100056

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