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

Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance.

Neurology - 22 Mar 2005

Pulkes T, Liolitsa D, Wills A J, Hargreaves I, Heales S, Hanna M G

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 Codon, Nonsense
Share to Electron Transport Complex I
Share to Exercise Tolerance
Share to Muscle Fibers, Skeletal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscle Weakness

Share to Muscular Diseases

Share to NADH Dehydrogenase

Share to Ophthalmoplegia

Source

Identifiers

PMID: 15781840
DOI: 10.1212/01.WNL.0000154471.33156.55

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance.PMID 15781840Read ↗

Mutations in mitochondrial DNA as a cause of exercise intolerance.Semantic proximity Read ↗

Sporadic myopathy and exercise intolerance associated with the mitochondrial 8328G>A tRNALys mutation.Semantic proximity Read ↗

Sudden death in non-syndromic mitochondrial disorders due to m.3243A > G may not only be cardiogenic.Semantic proximity Read ↗

Exercise-induced myalgia and rhabdomyolysis in a patient with the rare m.3243A>T mtDNA mutation.Semantic proximity Read ↗

Is mitochondrial disease the common cause of histiocytoid cardiomyopathy and non-compaction?Semantic proximity Read ↗

Hearing Loss in a Patient With the Myopathic Form of Mitochondrial DNA Depletion Syndrome and a Novel Mutation in the TK2 GeneSemantic proximity Read ↗

Somatic mutations in mitochondria: the chicken or the egg?Semantic proximity Read ↗

Mitochondrial miRNAs and fibromyalgia: new biomarker candidatesSemantic proximity Read ↗

A genetic polymorphism that is associated with mitochondrial energy metabolism increases risk of fibromyalgiaSemantic proximity Read ↗

The typical MERRF (A8344G) mutation of the mitochondrial DNA associated with depressive mood disorders.Semantic proximity Read ↗

Exercise intolerance due to mutations in the cytochrome b gene of mitochondrial DNA.Semantic proximity Read ↗

Decreased skeletal muscle mitochondrial DNA in patients with statin-induced myopathySemantic proximity Read ↗

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