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

Genes - 28 May 2022

Naveed Muhammad Asif, Abid Aiysha, Ali Nadir, Hassan Yaqoob, Amar Ali, Javed Aymen, Qamar Khansa, Mustafa Ghulam, Raza Ali, Saleem Umera, Hussain Shabbir, Shakoor Madiha, Khaliq Shagufta, Mohsin Shahida

Abstract excerpt

Type III von Willebrand disease is present in the Punjab province of Pakistan along with other inherited bleeding disorders like hemophilia. Cousin marriages are very common in Pakistan so genetic studies help to establish protocols for screening, especially at the antenatal level. Factors behind the phenotypic variation of the severity of bleeding in type III vWD are largely unknown. The study was conducted to...

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Identifiers

PMID: 35741733
DOI: 10.3390/genes13060971
PMCID: PMC9222927

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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.

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