Improved coagulation factor XIII B (FXIIIB) phenotyping after neuraminidase treatment of plasma and first description of the FXIIIB 2 phenotype
Author:
Publisher
Springer Science and Business Media LLC
Subject
Hematology,General Medicine,Hematology
Link
http://link.springer.com/content/pdf/10.1007/BF00319528.pdf
Reference18 articles.
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2. Barbui T, Cartei G, Chisesi T, Dine E (1974) Electroimmunoassay of plasma subunits-A and S in a case of congenital fibrin stabilizing factor deficiency. Thromb Diath Haemorrh 32: 124?131
3. Board PG (1979) Genetic polymorphism of the A subunit of human coagulation factor XIII. Am J Hum Genet 31: 116
4. Board PG (1980) Genetic polymorphism of the B subunit of human coagulation factor XIII. Am J Hum Genet 32: 348
5. Board PG, Coggan M, Hamer JW (1980) An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects. Br J Haematol 45: 633
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