Genotype-phenotype correlation in MYH9-related thrombocytopenia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2005.05658.x/fullpdf
Reference32 articles.
1. Expression of the Nonmuscle Myosin Heavy Chain IIA in the Human Kidney and Screening for MYH9 Mutations in Epstein and Fechtner Syndromes
2. Coexpression of May-Hegglin Anomaly and Hereditary Nephritis in a Family
3. Hereditary Nephritis Associated with May-Hegglin Anomaly
4. Defects in Cell Adhesion and the Visceral Endoderm following Ablation of Nonmuscle Myosin Heavy Chain II-A in Mice
5. Familial occurrence of the May-Hegglin anomaly: is the accompanying renal failure part of a new subentity?
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1. Unraveling MYH9-related disease: A case study on misdiagnosis with idiopathic thrombocytopenic purpura, confirmed through genetic;Heliyon;2024-09
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. Identification of a novel MYH9‐related disease‐associated mutation with multiple faintly staining Döhle‐like bodies;Pediatric Blood & Cancer;2024-07-04
4. A Case of Thrombocytopenia with <italic>MYH9</italic> Gene Mutation Found in Siblings;Soonchunhyang Medical Science;2024-06-30
5. Platelet genetic testing by next‐generation sequencing: A practical update;International Journal of Laboratory Hematology;2023-07-18
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