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Bernard‐Soulier syndrome in Pakistan: Biochemical and molecular analyses leading to identification of a novel mutation in <italic>GP1BA</italic>.
- Source :
- Haemophilia; Jan2018, Vol. 24 Issue 1, pe18-e22, 5p, 1 Diagram, 1 Chart
- Publication Year :
- 2018
-
Abstract
- The article discusses a study conducted on a cohort of Pakistani patients with severe bleeding abnormalities including hematoma, epistaxis and prolonged wound bleeding, who were diagnosed with Bernardâ€Soulier syndrome. According to the author, this disease is caused by defects to the platelet receptor for von Willebrand factor (VWF) and is accompanied by low platelet counts and impaired platelet agglutination after stimulation with ristocetin.
Details
- Language :
- English
- ISSN :
- 13518216
- Volume :
- 24
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Haemophilia
- Publication Type :
- Academic Journal
- Accession number :
- 127390517
- Full Text :
- https://doi.org/10.1111/hae.13365