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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...

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Bibliografske podrobnosti
Main Authors: Shapiro, Sandor S., Martinez, Jose, Holburn, Ruth R.
Format: Artigo
Jezik:Inglês
Izdano: 1969
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC297482/
https://ncbi.nlm.nih.gov/pubmed/5355338
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