Clinical, Pathological, and Genetic Analysis of Ten Patients with MYH9-Related Disease
Author:
Publisher
S. Karger AG
Subject
Hematology,General Medicine
Reference31 articles.
1. Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease
2. Nonmuscle Myosin Heavy Chain IIA Mutations Define a Spectrum of Autosomal Dominant Macrothrombocytopenias: May-Hegglin Anomaly and Fechtner, Sebastian, Epstein, and Alport-Like Syndromes
3. MYH9-Related Platelet Disorders
4. Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13
5. Mapping of a gene for May-Hegglin anomaly to chromosome 22q
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