Phenotype onset in Huntington’s disease knock‐in mice is correlated with the incomplete splicing of the mutant huntingtin gene

Huntington’s disease (HD) is a progressive neurodegenerative disorder caused by an expanded CAG repeat within the huntingtin (HTT) gene. The Q140 and HdhQ150 knock‐in HD mouse models were generated such that HdhQ150 mice have an expanded CAG repeat inserted into the mouse Htt gene, whereas in the Q1...

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Detalles Bibliográficos
Autores principales: Franich, Nicholas R., Hickey, Miriam A., Zhu, Chunni, Osborne, Georgina F., Ali, Nadira, Chu, Tiffany, Bove, Nicholas H., Lemesre, Vincent, Lerner, Renata P., Zeitlin, Scott O., Howland, David, Neueder, Andreas, Landles, Christian, Bates, Gillian P., Chesselet, Marie‐Francoise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Huntington's Disease
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801054/
https://www.ncbi.nlm.nih.gov/pubmed/31282030
http://dx.doi.org/10.1002/jnr.24493

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801054/
https://www.ncbi.nlm.nih.gov/pubmed/31282030
http://dx.doi.org/10.1002/jnr.24493

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