Debiec, Hanna <br/><br/>
Role of truncating mutations in MME gene in fetomaternal alloimmunisation and antenatal glomerulopathies.  [electronic resource] 

 -  Lancet (London, England)   
 - 1252-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1474-547X 
<br/><br/><label>Standard No.: </label>10.1016/S0140-6736(04)17142-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Antigen-Antibody Complex--analysis<br/>Child, Preschool<br/>Female<br/>Fetal Diseases--genetics<br/>Fetomaternal Transfusion--immunology<br/>Glomerulonephritis, Membranous--congenital<br/>Humans<br/>Immunization<br/>Immunoglobulin G--analysis<br/>Infant, Newborn<br/>Isoantibodies--immunology<br/>Kidney Glomerulus--immunology<br/>Mutation<br/>Neprilysin--deficiency<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide<br/>Pregnancy