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Cell-Autonomous and Non-cell-Autonomous Pathogenic Mechanisms in Huntington’s Disease: Insights from In Vitro and In Vivo Models

Huntington’s disease (HD) is an autosomal dominant disorder caused by an expansion in the trinucleotide CAG repeat in exon-1 in the huntingtin gene, located on chromosome 4. When the number of trinucleotide CAG exceeds 40 repeats, disease invariably is manifested, characterized by motor, cognitive,...

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Publicat a:Neurotherapeutics
Autors principals: Creus-Muncunill, Jordi, Ehrlich, Michelle E.
Format: Artigo
Idioma:Inglês
Publicat: Springer International Publishing 2019
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6985401/
https://ncbi.nlm.nih.gov/pubmed/31529216
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-019-00782-9
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