Falcão, D A <br/><br/>
Deficiency of the human complement regulatory protein factor H associated with low levels of component C9.  [electronic resource] 

 -  Scandinavian journal of immunology  Oct 2008 
 - 445-55 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1365-3083 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-3083.2008.02152.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Blood Coagulation Disorders, Inherited--blood<br/>Blotting, Western<br/>Child, Preschool<br/>Complement Activation--physiology<br/>Complement C3b Inactivator Proteins<br/>Complement C9--analysis<br/>Complement Factor H--deficiency<br/>Complement System Proteins--analysis<br/>Consanguinity<br/>Enzyme-Linked Immunosorbent Assay<br/>Female<br/>Fibroblasts--metabolism<br/>Humans<br/>Male<br/>Microscopy, Confocal<br/>Mutation<br/>Pedigree<br/>Pneumonia--etiology<br/>Reverse Transcriptase Polymerase Chain Reaction