Neumann, H P H <br/><br/>
Haemolytic uraemic syndrome and mutations of the factor H gene: a registry-based study of German speaking countries.  [electronic resource] 

 -  Journal of medical genetics  Sep 2003 
 - 676-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.40.9.676  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Austria<br/>Complement C3--metabolism<br/>Complement Factor H--genetics<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Enzyme-Linked Immunosorbent Assay<br/>Female<br/>Germany<br/>Hemolytic-Uremic Syndrome--blood<br/>Humans<br/>Italy<br/>Kidney Failure, Chronic--complications<br/>Kidney Transplantation<br/>Male<br/>Mutation<br/>Polymorphism, Single-Stranded Conformational<br/>Registries--statistics & numerical data<br/>Switzerland