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Article

Defining and refining the phenotype of PRRT2 mutations.

Developmental medicine and child neurology - 1 Apr 2013

Mink Jonathan W

Abstract excerpt

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Topics

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Share to Dyskinesias
Share to Epilepsy, Benign Neonatal
Share to PRRT2 gene
Share to Membrane Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Nerve Tissue Proteins

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Source

Identifiers

PMID: 23362825
DOI: 10.1111/dmcn.12101

Genes

PRRT2

Provenance

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