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

Coronary Artery Disease in Heterozygous Familial Hypercholesterolemia Patients With the Same LDL Receptor Gene Mutation

1 Aug 1995

Abstract excerpt

BACKGROUND: Familial hypercholesterolemia (FH), an autosomal codominant disease, is characterized by high levels of LDL cholesterol and a high incidence of coronary artery disease (CAD). To date, genetic heterogeneity has hindered the proper assessment of the relation between risk factors and CAD in FH patients. METHODS AND RESULTS: We studied the association between CAD and common risk factors in a sample of 263...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Diabetes, Cardiovascular Risks, and Lipoproteins
Share to Lipid metabolism and disorders
Share to Lipoproteins and Cardiovascular Health

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

Source

Identifiers

PMID: 7634440
DOI: 10.1161/01.cir.92.3.290

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 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

Coronary Artery Disease in Heterozygous Familial Hypercholesterolemia Patients With the Same LDL Receptor Gene MutationPMID 7634440Read ↗

The genetic basis of familial hypercholesterolemia: inheritance, linkage, and mutationsSemantic proximity Read ↗

Heterozygous familial hypercholesterolemia: an underrecognized cause of early cardiovascular diseaseSemantic proximity Read ↗

Genetic Counseling and Genetic Testing for Familial HypercholesterolemiaSemantic proximity Read ↗

Clinical expression of familial hypercholesterolemia in clusters of mutations of the LDL receptor gene that cause a receptor-defective or receptor-negative phenotype.Semantic proximity Read ↗

Clinical, diagnostic, and therapeutic aspects of familial hypercholesterolemia.Semantic proximity Read ↗

Differences in characteristics and risk of cardiovascular disease in familial hypercholesterolemia patients with and without tendon xanthomas: a systematic review and meta-analysis.Semantic proximity Read ↗

Phenotypic variation in heterozygous familial hypercholesterolemia: a comparison of Chinese patients with the same or similar mutations in the LDL receptor gene in China or Canada.Semantic proximity Read ↗

[Familial hypercholesterolemia: A largely underestimated cardiovascular risk].Semantic proximity Read ↗

Genetic susceptibility to heart disease in Canada: lessons from patients with familial hypercholesterolemia.Semantic proximity Read ↗

Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society.Semantic proximity Read ↗

[Molecular genetic causes of familial hypercholesterolemia].Semantic proximity Read ↗

Variable phenotype associated with compound LDLR gene mutations in familial hypercholesterolemia patients: Case series and clinical implications.Semantic proximity Read ↗

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