Advances in the understanding of MYH9 disorders
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference52 articles.
1. Historical hematology: May–Hegglin anomaly
2. Mutation of MYH9, encoding non-muscle myosin heavy chain A, in May-Hegglin anomaly
3. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
4. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
5. Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes
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1. Inherited Leukocyte Disorders;Pediatric Pathology of Hematopoietic and Histiocytic Disorders;2024-02-15
2. Nonmuscle Myosin IIA Regulates the Precise Alignment of Hexagonal Eye Lens Epithelial Cells During Fiber Cell Formation and Differentiation;Investigative Opthalmology & Visual Science;2023-04-18
3. Successful administration of eltrombopag in preparation for peritoneal dialysis catheter placement in a girl with MYH9-related disease;CEN Case Reports;2023-03-31
4. Renal injury associated with MYH9 disorder with 5773delG mutation: A case report;Clinical Nephrology;2023-03-01
5. Systematic identification of intron retention associated variants from massive publicly available transcriptome sequencing data;Nature Communications;2022-09-29
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