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Characterization of a Variant Prothrombin in a Patient Congenitally Deficient in Factors II, VII, IX and X

✍ Scribed by C. A. Johnson; K. S. Chung; K. M. McGrath; P. E. Bean; H. R. Roberts


Book ID
114709261
Publisher
John Wiley and Sons
Year
1980
Tongue
English
Weight
600 KB
Volume
44
Category
Article
ISSN
0007-1048

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M.D.P.); and lmmuno A.G., Vienna, Austria (M.K.) Hereditary factor VII deficiency is a rare autosomal recessive condition, usually associated with normal or reduced levels of a functionally defective molecule. The available means of treating thiscondition in North America presents serious health ri