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Article

Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations.

Movement disorders : official journal of the Movement Disorder Society - 1 Jan 2012

Hinnell Claire, Haider Salman, Delamont Shane, Clough Chris, Hadzic Nedim, Samuel Michael

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Share to DNA-Directed DNA Polymerase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21956653
DOI: 10.1002/mds.23960

Genes

POLG

Provenance

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

Related research

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Research trail→

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Dystonia in mitochondrial spinocerebellar ataxia and epilepsy syndrome associated with novel recessive POLG mutations.PMID 21956653Read ↗

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations.Semantic proximity Read ↗

Novel POLG mutation in a patient with sensory ataxia, neuropathy, ophthalmoparesis and stroke.Semantic proximity Read ↗

POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.Semantic proximity Read ↗

Ataxia with ophthalmoplegia or sensory neuropathy is frequently caused by POLG mutations.Semantic proximity Read ↗

Early-onset parkinsonism due to compound heterozygous POLG mutations.Semantic proximity Read ↗

Clinical and Molecular Features of POLG-Related Sensory Ataxic Neuropathy with Dysarthria and Ophthalmoparesis.Semantic proximity Read ↗

Complex hyperkinetic movement disorders associated with POLG mutations.Semantic proximity Read ↗

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype in a patient with a novel heterozygous POLG mutation.Semantic proximity Read ↗

Clinical and molecular features of POLG-related mitochondrial disease.Semantic proximity Read ↗

A Scoping Review of POLG-Related Cerebellar Ataxia: Insights and Clinical Perspectives.Semantic proximity Read ↗

Juvenile dystonia-parkinsonism and dementia caused by a novel ATP13A2 frameshift mutationSemantic proximity Read ↗

[Adult-onset sensory neuropathy and ataxia as a clinical manifestation of POLG gene mutations].Semantic proximity Read ↗

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