Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Complex hyperkinetic movement disorders associated with POLG mutations.

Movement disorders : official journal of the Movement Disorder Society - 30 Oct 2010

Synofzik Matthis, Schüle Rebecca, Schulte Claudia, Krüger Rejko, Lindig Tobias, Schöls Ludger, Asmus Friedrich

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA-Directed DNA Polymerase
Share to DNA Polymerase gamma
Share to POLG gene
Share to Hyperkinesis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Mutation

Share to Pedigree

Source

Identifiers

PMID: 20818669
DOI: 10.1002/mds.23307

Genes

POLG

Provenance

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

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complex hyperkinetic movement disorders associated with POLG mutations.PMID 20818669Read ↗

Emerging Monogenic Complex Hyperkinetic Disorders.Semantic proximity Read ↗

Neuromuscular Disorders: Clinical and Molecular GeneticsSemantic proximity Read ↗

Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations.Semantic proximity Read ↗

Movement disorders in 2014. Genetic advances spark a revolution in dystonia phenotyping.Semantic proximity Read ↗

Complex movement disorders associated with DEAF1 gene mutation.Semantic proximity Read ↗

Movement disorders in 2016: from genes to phenotypes.Semantic proximity Read ↗

Postsynaptic movement disorders: clinical phenotypes, genotypes, and disease mechanisms.Semantic proximity Read ↗

Movement disorders associated with hyperthyroidism: expanding the phenotype.Semantic proximity Read ↗

Genetics of Movement Disorders and the Practicing Clinician; Who and What to Test for?Semantic proximity Read ↗

Movement disorders associated with thiamine pyrophosphokinase deficiency: Intrafamilial variability in the phenotype.Semantic proximity Read ↗

Concentric muscle involvement in POLG-related distal myopathy.Semantic proximity Read ↗

"Dancing feet dyskinesias": a clue to parkin gene mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.