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Article

A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients.

Hong Kong medical journal = Xianggang yi xue za zhi - 1 Dec 2016

Law C Y, Yeung W L, Cheung Y F, Chan H F, Fung E, Hui J, Yung I Ok, Yuen Y P, Chan A Ok, Lam C W

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 27920401
DOI: 10.12809/hkmj154579

Genes

PRRT2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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A common PRRT2 mutation in familial paroxysmal kinesigenic dyskinesia in Hong Kong: a case series of 16 patients.PMID 27920401Read ↗

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Novel loss-of-function PRRT2 mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese family.Semantic proximity Read ↗

[Clinical features and PRRT2 gene mutation in paroxysmal kinesigenic dyskinesia].Semantic proximity Read ↗

Clinical characteristics and PRRT2 gene mutation analysis of sporadic patients with paroxysmal kinesigenic dyskinesia in China.Semantic proximity Read ↗

PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia.Semantic proximity Read ↗

Paroxysmal kinesigenic dyskinesia: clinical report of 10 cases from three pedigrees with literature review.Semantic proximity Read ↗

PRRT2 Mutations in Paroxysmal Kinesigenic Dyskinesia with Infantile Convulsions in a Taiwanese CohortSemantic proximity Read ↗

PRRT2 mutations in a cohort of Chinese families with paroxysmal kinesigenic dyskinesia and genotype-phenotype correlation reanalysis in literatures.Semantic proximity Read ↗

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