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Article

Codon 101 of PRKCG, a preferential mutation site in SCA14.

Movement disorders : official journal of the Movement Disorder Society - 15 Sept 2007

Nolte Dagmar, Klebe Stephan, Baron Ralf, Deuschl Günther, Müller Ulrich

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Identifiers

PMID: 17659643
DOI: 10.1002/mds.21654

Genes

PRKCG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

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