Iwamoto, K <br/><br/>
A large heterozygous deletion including the entire C1 inhibitor gene in a sporadic case of hereditary angio-oedema.  [electronic resource] 

 -  Clinical and experimental dermatology  Jan 2012 
 - 20-3 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1365-2230 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2230.2011.04138.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Angioedemas, Hereditary--blood<br/>Asian People<br/>Complement C1 Inhibitor Protein--genetics<br/>Exons--genetics<br/>Female<br/>Fibrin Fibrinogen Degradation Products--analysis<br/>Genetic Predisposition to Disease<br/>Humans<br/>Real-Time Polymerase Chain Reaction<br/>Sequence Deletion