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Article

Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.

Movement disorders : official journal of the Movement Disorder Society - 31 Oct 2007

Wieczorek Stefan, Arning Larissa, Gizewski Elke R, Alheite Ingrid, Timmann Duymal

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17708558
DOI: 10.1002/mds.21673

Genes

PRKCG

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene.PMID 17708558Read ↗

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