Thrombin generation in two families with MYH9-related platelet disorder
Author:
Publisher
Informa UK Limited
Subject
Hematology,General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/09537104.2015.1064882
Reference11 articles.
1. Mutation spectrum and genotype‐phenotype correlations in a large French cohort of MYH 9‐Related Disorders
2. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
3. MYH-9 Related Platelet Disorders: Strategies for Management and Diagnosis
4. Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May–Hegglin, Sebastian, Fechtner and Epstein syndromes)
5. Functional compensation of the low platelet count by increased individual platelet size in a patient with May-Hegglin anomaly presenting with acute myocardial infarction
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