Kloss-Brandstätter, Anita <br/><br/>
Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.  [electronic resource] 

 -  PloS one  2012 
 - e35015 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0035015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anemia, Iron-Deficiency--blood<br/>Cation Transport Proteins--genetics<br/>Child<br/>Child, Preschool<br/>Dietary Supplements<br/>Female<br/>Ferritins--blood<br/>Genetic Association Studies<br/>Haplotypes<br/>Humans<br/>Infant<br/>Iron--blood<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation<br/>Pedigree<br/>Polymorphism, Single Nucleotide<br/>Serbia<br/>Serine Endopeptidases--genetics