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Article

Molecular and clinical profile of type 2 von Willebrand disease in Iran: a thirteen-year experience.

International journal of hematology - 1 Apr 2020

Rassoulzadegan Maryam, Ala Fereydoun, Jazebi Mohammad, Enayat Mohammad Said, Tabibian Shadi, Shams Mahmood, Bahraini Mehran, Dorgalaleh Akbar

Abstract excerpt

Type 2 von Willebrand disease (VWD) is the most common congenital bleeding disorder, with variable bleeding tendency and a complex laboratory phenotype. In the current study, we report the clinical and molecular profile of a large number of Iranian patients with type 2 VWD. All exons, intron-exon boundaries, and untranslated regions were sequenced by Sanger sequencing for direct mutation detection. All identified...

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PMID: 31939074
DOI: 10.1007/s12185-019-02814-8

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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.

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