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 dysfunction in a case of fatal infantile cardiomyopathy.

Journal of inherited metabolic disease - 1 Jan 1994

Marin-Garcia J, Ananthakrishnan R, Carta M, Dubois R, Gu J, Goldenthal M J

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 Fatal Outcome
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mitochondria

Share to Mutation

Source

Identifiers

PMID: 7707704
DOI: 10.1007/BF00712023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mitochondrial dysfunction in a case of fatal infantile cardiomyopathy.PMID 7707704Read ↗

Mitochondrial mutation in fatal infantile cardiomyopathy.Semantic proximity Read ↗

Infantile mitochondrial disorders.Semantic proximity Read ↗

Mitochondrial cardiomyopathy: molecular and biochemical analysis.Semantic proximity Read ↗

Novel mutations in mitochondrial cytochrome b in fatal post partum cardiomyopathy.Semantic proximity Read ↗

Inborn and induced defects of the mitochondrial respiratory chain.Semantic proximity Read ↗

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

Giant Mitochondria in the Myocardium of a Patient With Mitochondrial CardiomyopathySemantic proximity Read ↗

AIFM1 mutation presenting with fatal encephalomyopathy and mitochondrial disease in an infant.Semantic proximity Read ↗

Mitochondrial function in children with idiopathic dilated cardiomyopathy.Semantic proximity Read ↗

Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy.Semantic proximity Read ↗

Severe infantile parkinsonism because of a de novo mutation on DLP1 mitochondrial-peroxisomal protein.Semantic proximity Read ↗

Mitochondrial disorder associated with newborn cardiopulmonary arrest.Semantic proximity Read ↗

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