Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation. [electronic resource]
Producer: 20120807Description: e35015 p. digitalISSN:- 1932-6203
- Adult
- Anemia, Iron-Deficiency -- blood
- Cation Transport Proteins -- genetics
- Child
- Child, Preschool
- Dietary Supplements
- Female
- Ferritins -- blood
- Genetic Association Studies
- Haplotypes
- Humans
- Infant
- Iron -- blood
- Male
- Membrane Proteins -- genetics
- Mutation
- Pedigree
- Polymorphism, Single Nucleotide
- Serbia
- Serine Endopeptidases -- genetics
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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