A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization (Q38334302)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization |
scientific article |
Statements
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A congenitally abnormal fibrinogen (Vlissingen) with a 6-base deletion in the gamma-chain gene, causing defective calcium binding and impaired fibrin polymerization (English)
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Koopman J
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Haverkate F
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Briët E
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Lord ST
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1 July 1991
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266
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20
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13456-13461
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Identifiers
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