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Article

Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.

Movement disorders : official journal of the Movement Disorder Society - 1 Nov 2006

Stefanova Elka, Djarmati Ana, Momcilović Dragana, Dragasević Natasa, Svetel Marina, Klein Christine, Kostić Vladimir S

Abstract excerpt

The aim of this study was to describe the clinical features of a large Serbian family with paroxysmal nonkinesigenic dyskinesia (PNKD) and one of the two previously described mutations in the Myofibrillogenesis regulator 1 gene (MR-1), which causes an alanine-to-valine substitution at position 9....

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Identifiers

PMID: 16972263
DOI: 10.1002/mds.21095

Genes

PNKD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-16972263-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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