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 <i>PRKC...

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Bibliographic Details
Main Authors: Szilvia E. Mezey, Josef P. Kapfhammer, Etsuko Shimobayashi
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/13/8/1417