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

Mitochondrial cardiomyopathy due to m.3243A>G mitochondrial DNA mutation presenting in late adulthood: a case report.

Hong Kong medical journal = Xianggang yi xue za zhi - 1 Jun 2020

Chau E M C, Ma E S K, Chan A O O, Tsoi T H, Law W L

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 Cardiomyopathy, Hypertrophic
Share to DNA, Mitochondrial
Share to Mitochondrial Diseases
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Source

Identifiers

PMID: 32554818
DOI: 10.12809/hkmj198051

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial cardiomyopathy due to m.3243A>G mitochondrial DNA mutation presenting in late adulthood: a case report.PMID 32554818Read ↗

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.Semantic proximity Read ↗

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

Mitochondrial disease caused by the m.3243A>G mutationSemantic proximity Read ↗

Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).Semantic proximity Read ↗

The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.Semantic proximity Read ↗

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.Semantic proximity Read ↗

[Mitochondrial DNA mutations and cardiomyopathy].Semantic proximity Read ↗

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load.Semantic proximity Read ↗

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management.Semantic proximity Read ↗

Expanding the clinical phenotype of the mitochondrial m.13513G>A mutation with the first report of a fatal neonatal presentation: importance of DNA collection for post-mortem diagnosis.Semantic proximity Read ↗

[A3243G mitochondrial DNA mutation and heterogeneous phenotypic expression].Semantic proximity Read ↗

Mitochondrial A3243G mutation with manifestation of acute dilated cardiomyopathy.Semantic proximity Read ↗

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