Candidate Gene Sequencing of SLC11A2 and TMPRSS6 in a Family with Severe Anaemia: Common SNPs, Rare Haplotypes, No Causative Mutation
Table 1
Laboratory parameters of the family at the time of taking of the first blood samples, and after intravenous iron administrations in the family's children suffering from IRIDA, i.e. Son 2, and Daughters 1 and 2.