Juvenile Huntington’s Disease and Other PolyQ Diseases, Update on Neurodevelopmental Character and Comparative Bioinformatic Review of Transcriptomic and Proteomic Data

Polyglutamine (PolyQ) diseases are neurodegenerative disorders caused by the CAG repeat expansion mutation in affected genes resulting in toxic proteins containing a long chain of glutamines. There are nine PolyQ diseases: Huntington’s disease (HD), spinocerebellar ataxias (types 1, 2, 3, 6, 7, and...

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Detalles Bibliográficos
Autores principales: Świtońska-Kurkowska, Karolina, Krist, Bart, Delimata, Joanna, Figiel, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281051/
https://www.ncbi.nlm.nih.gov/pubmed/34277598
http://dx.doi.org/10.3389/fcell.2021.642773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281051/
https://www.ncbi.nlm.nih.gov/pubmed/34277598
http://dx.doi.org/10.3389/fcell.2021.642773

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