Genetically Confirmed Dual Hematologic Disorder: A Case of β-Thalassemia with Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient
Year: 2025
Type: article
Study design: Case Report
Source: Hemoglobin
Authors: Muhammad Tariq Masood Khan, Ihtisham Ul Haq, Ihtisham Ul Haq, Aamir Ali, Inam Ul Haq, Inam Ul Haq, Afaq Ahmad
Institutions: Pak International Medical College, Rehman Medical Institute
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W4415984823