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Ataxin-3, The Spinocerebellar Ataxia Type 3 Neurodegenerative Disorder Protein, Affects Mast Cell Functions

Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph Disease, is a progressive neurodegenerative disorder characterized by loss of neuronal matter due to the expansion of the CAG repeat in the ATXN3/MJD1 gene and subsequent ataxin-3 protein. Although the underlying pathogenic protein e...

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Detalles Bibliográficos
Autores principales: Sowa, Anna S., Haas, Eva, Hübener-Schmid, Jeannette, Lorentz, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086395/
https://www.ncbi.nlm.nih.gov/pubmed/35558088
http://dx.doi.org/10.3389/fimmu.2022.870966