Associated Papers
Non-synonymous SNPs variants of PRKCG and its association with oncogenes predispose to hepatocellular carcinoma.
Abid F et al.
Cancer Cell International, 2023
Novel mutation in exon11 of PRKCG (SCA14): A case report.
Sun R et al.
Frontiers in Genetics, 2023
Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations.
De Michele G et al.
Journal of Neurology, 2022
Spinocerebellar ataxia type 14: refining clinicogenetic diagnosis in a rare adult-onset disorder.
Schmitz-Hübsch T et al.
Annals of Clinical and Translational Neurology, 2021
33739604 (PubMed )
Supplement: ACN3-8-774-s001.xlsx › summary_content
High Degree of Genetic Heterogeneity for Hereditary Cerebellar Ataxias in Australia.
Kang C et al.
Cerebellum (london, England), 2019
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