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

Association between Genetic Polymorphism and Risk of von Willebrand Disease in Pakistan.

BioMed research international - 1 Jan 2017

Arshad Najma, Nawaz Syed Kashif, Iqbal Riffat, Arshad Muhammad, Musheer Farhana, Naz Amber, Mushtaq Iqra, Jaleel Sara

Abstract excerpt

von Willebrand disease (VWD) is an inherited, genetically and clinically heterogeneous hemorrhagic disorder. The most common cause of this disease is mutation in the gene that encodes protein von Willebrand factor (VWF) which is responsible for blood clotting. The current study was designed to investigate the role of genetic polymorphisms with the onset of VWD in population of Pakistan. Three exonic variants...

Read the complete abstract on PubMed

Topics

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

Share to Alleles
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pakistan

Share to Polymorphism, Single Nucleotide

Share to von Willebrand Diseases

Share to von Willebrand Factor

Source

Open in PubMed Open full text

Identifiers

PMID: 29423401
DOI: 10.1155/2017/1070471
PMCID: PMC5750513

Genes

VWF

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association between Genetic Polymorphism and Risk of von Willebrand Disease in Pakistan.PMID 29423401Read ↗

Molecular characterization of exon 28 of von Willebrand's factor gene in Nigerian population.Semantic proximity Read ↗

Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease.Semantic proximity Read ↗

[Relationship of von Willebrand factor gene single-nucleotide polymorphism with thrombosis diseases].Semantic proximity Read ↗

Autosomal recessive inherited bleeding disorders in Pakistan: a cross-sectional study from selected regionsSemantic proximity Read ↗

Associations of multiple genetic variations with plasma levels of Von Willebrand Factor and clinical phenotype in Iranian patients with Von Willebrand disease type 1.Semantic proximity Read ↗

A standard nomenclature for von Willebrand factor gene mutations and polymorphisms. On behalf of the ISTH SSC Subcommittee on von Willebrand factor.Semantic proximity Read ↗

Impact of thrombogenic mutations on clinical phenotypes of von Willebrand disease.Semantic proximity Read ↗

Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: a review.Semantic proximity Read ↗

Epidemiology, diagnosis, and management of von Willebrand disease in India.Semantic proximity Read ↗

von Willebrand disease in China.Semantic proximity Read ↗

[The phenotypic and genotypic diagnosis of three Chinese patients with von Willebrand disease].Semantic proximity Read ↗

Characterizing polymorphisms and allelic diversity of von Willebrand factor gene in the 1000 Genomes.Semantic proximity Read ↗

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