A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization
Open Access
- 1 July 1991
- journal article
- case report
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 266 (20) , 13456-13461
- https://doi.org/10.1016/s0021-9258(18)98861-7
Abstract
No abstract availableKeywords
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