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

[Phenotype variation of familial hypertrophic cardiomyopathy caused by combined missense mutations].

Nihon Hoshasen Gijutsu Gakkai zasshi - 1 Mar 2002

Arai Shoichi

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, Familial
Share to Mitochondria
Share to Mutation, Missense
Share to Myosin Heavy Chains

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Polymorphism, Genetic

Share to Troponin T

Source

Identifiers

PMID: 12564437
DOI: 10.6009/jjrt.kj00001364299

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

[Phenotype variation of familial hypertrophic cardiomyopathy caused by combined missense mutations].PMID 12564437Read ↗

[Genetic analysis of hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Genetics of hypertrophic cardiomyopathies].Semantic proximity Read ↗

[Hypertrophic cardiomyopathy: New pathogenic variant in MYH7].Semantic proximity Read ↗

[Genotype-phenotype correlations in familial hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Hypertrophic cardiomyopathy with restrictive phenotype: a case report].Semantic proximity Read ↗

Different clinical presentation, cardiac morphology and gene mutations in two sisters with hypertrophic cardiomyopathy-A case report.Semantic proximity Read ↗

[Genetic aspects of myocardial hypertrophy in hypertrophic cardiomyopathy and arterial hypertension].Semantic proximity Read ↗

[One patient, one mutation and two cardiomyopathies - hypertrophic cardiomyopathy and left ventricular noncompaction].Semantic proximity Read ↗

[Recent research developments on associations between disease-causing genes and metabolic hypertrophic cardiomyopathy.].Semantic proximity Read ↗

[Cardiac phenotype in patients with hereditary neuromuscular disease: from molecular genetics to the bedside].Semantic proximity Read ↗

[Research progress on the association of cardiac ion channel gene variants with hypertrophic cardiomyopathy and related arrhythmias].Semantic proximity Read ↗

Overlapping Phenotype of Cardiomyopathy in Patient With Double MutationSemantic proximity Read ↗

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