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Transcriptome Profile of a New Mouse Model of Spinocerebellar Ataxia Type 14 Implies Changes in Cerebellar Development

The autosomal dominant inherited spinocerebellar ataxias (SCAs) are a group of neurodegenerative disorders characterized by cerebellar atrophy and loss of Purkinje neurons. Spinocerebellar ataxia type 14 (SCA14) is a rare variant of SCAs caused by missense mutations or deletions in the PRKCG gene en...

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Detalles Bibliográficos
Autores principales:	Mezey, Szilvia E., Kapfhammer, Josef P., Shimobayashi, Etsuko
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407720/ https://www.ncbi.nlm.nih.gov/pubmed/36011327 http://dx.doi.org/10.3390/genes13081417

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