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

Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chains

31 Jan 2019

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 and Myosin Studies
Share to Cardiovascular Effects of Exercise
Share to Muscle Physiology and Disorders

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 30706179
DOI: 10.1007/s00424-019-02257-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 21 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hereditary heart disease: pathophysiology, clinical presentation, and animal models of HCM, RCM, and DCM associated with mutations in cardiac myosin light chainsPMID 30706179Read ↗

Molecular mechanisms in cardiomyopathy.Semantic proximity Read ↗

Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutations.Semantic proximity Read ↗

Molecular and clinical aspects of inherited cardiomyopathies.Semantic proximity Read ↗

Genetic mutations and mechanisms in dilated cardiomyopathy.Semantic proximity Read ↗

Phenotypic variation and targeted therapy of hypertrophic cardiomyopathy using genetic animal models.Semantic proximity Read ↗

Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscleSemantic proximity Read ↗

Molecular Mechanisms of Inherited CardiomyopathiesSemantic proximity Read ↗

Mitochondrial DNA related cardiomyopathies.Semantic proximity Read ↗

Understanding cardiomyopathy phenotypes based on the functional impact of mutations in the myosin motor.Semantic proximity Read ↗

Diagnosis and management of inherited cardiomyopathies.Semantic proximity Read ↗

Restrictive cardiomyopathy: from genetics and clinical overview to animal modeling.Semantic proximity Read ↗

From sarcomeric mutations to heart disease: understanding familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

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