Avatrombopag improves thrombocytopenia in MYH9-related disorder following eltrombopag treatment failure
Author:
Affiliation:
1. School of International Education, Jianghan University, Wuhan, P.R. China
2. Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, P.R. China
Funder
the Natural Science Foundation of Hubei Province
Publisher
Informa UK Limited
Subject
Hematology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/09537104.2022.2096211
Reference25 articles.
1. Human Nonsyndromic Hereditary Deafness DFNA17 Is Due to a Mutation in Nonmuscle Myosin MYH9
2. Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome)
3. Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes
4. Global Variome shared LOVD. The MYH9 Gene Homepage. [accessed 2022 Feb 13]. https://databases.lovd.nl/shared/genes/MYH9.
5. Dynamic Visualization of Thrombopoiesis Within Bone Marrow
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