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RUNX1-FPDMM in families with mild thrombocytopenia and platelet function anomalies: a case series
ORIGINAL RESEARCH article Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1657054 This article is part of the Research TopicInherited or Acquired Defects in Primary and Secondary HemostasisView all 3 articles 1 Introduction Inherited platelet disorders (IPDs) are a diverse group of conditions that affect platelet count and often platelet function.
Diseases | Free Full-Text | Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the ITGA2B Gene
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