Heinen, Stefan <br/><br/>
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.  [electronic resource] 

 -  Human mutation  Mar 2006 
 - 292-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.9408  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Chromosomes, Human, Pair 1<br/>Cohort Studies<br/>Complement Factor H--genetics<br/>Erythrocytes--cytology<br/>Gene Conversion<br/>Hemolytic-Uremic Syndrome--genetics<br/>Humans<br/>Models, Genetic<br/>Molecular Sequence Data<br/>Multigene Family<br/>Mutation<br/>Sequence Homology, Nucleic Acid<br/>Sheep