Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.

Kloss-Brandstätter, Anita

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

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1932-6203

10.1371/journal.pone.0035015 doi


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