Novel mutation in exon11 of PRKCG (SCA14): A case report

Overview of attention for article published in Frontiers in Genetics, March 2023

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Novel mutation in exon11 of PRKCG (SCA14): A case report https://t.co/vEJGW6pdJ6 https://t.co/Q0JS8PaJiG

11 Mar 2023

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New Research: Novel mutation in exon11 of PRKCG (SCA14): A case report: Introduction:PRKCG mutations have been implicated in the pathogenesis of spinocerebellar ataxia type 14 (SCA14), which is a rare autosomal dominant disease marked by… https://t.co/F0B9

08 Mar 2023

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