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Congenital dysprothrombinemia: an inherited structural disorder of human prothrombin
A large family has been studied, 11 of whose members have half-normal plasma concentrations of biological prothrombin activity. The pattern of inheritance is autosomal. By use of a specific immunoassay, affected family members have been shown to possess normal quantities of immunoreactive prothrombi...
Uloženo v:
| Vydáno v: | J Clin Invest |
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| Hlavní autoři: | , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Society for Clinical Investigation
1969
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC297482/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/5355338/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI106191 |
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