Loreth, R M <br/><br/>
Fibrinogen kaiserslautern III: a new case of congenital dysfibrinogenemia with aalpha 16 arg-->cys substitution.  [electronic resource] 

 -  Haemostasis   
 - 12-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0301-0147 
<br/><br/><label>Standard No.: </label>10.1159/000048039  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Blood Coagulation Disorders--congenital<br/>Blood Coagulation Tests<br/>Family Health<br/>Fibrinogens, Abnormal--genetics<br/>Fibrinopeptide A--metabolism<br/>Fibrinopeptide B--metabolism<br/>Hemorrhage--etiology<br/>Humans<br/>Male<br/>Middle Aged<br/>Point Mutation<br/>Sequence Analysis, DNA<br/>Thrombin--pharmacology