R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference15 articles.
1. Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome;Deutsch;Blood,2003
2. MYH9-related platelet disorders;Althaus;Semin Thromb Hemost,2009
3. Description of a novel mutation leading to MYH9-related disease;Burt;Thromb Res,2008
4. Historical hematology: May-Hegglin anomaly;Saito;Am J Hematol,2008
5. Perioperative management of a patient with May-Hegglin anomaly requiring craniotomy;Sehbai;Am J Hematol,2005
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1. Exploring the nexus between MYH9 and tumors: novel insights and new therapeutic opportunities;Frontiers in Cell and Developmental Biology;2024-08-01
2. MYH9-related inherited thrombocytopenia: the genetic spectrum, underlying mechanisms, clinical phenotypes, diagnosis, and management approaches;Research and Practice in Thrombosis and Haemostasis;2024-08
3. Qualitative platelet alterations in May — Hegglin anomaly;Russian journal of hematology and transfusiology;2023-11-16
4. QUALITATIVE PLATELET ALTERATIONS IN MAY - HEGGLIN ANOMALY;GEMATOL TRANSFUZIOL;2023
5. May–Hegglin anomaly: A rare hereditary autoimmune thrombocytopenia;Indian Journal of Health Sciences and Biomedical Research (KLEU);2023
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