Candidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation.
Kloss-Brandstätter A, Erhart G, Lamina C, Meister B, Haun M, Coassin S, Seifert M, Klein-Franke A, Paulweber B, Kedenko L, Kollerits B, Swinkels DW, Vermeulen SH, Galesloot TE, Kronenberg F, Weiss G.
Kloss-Brandstätter A, et al. Among authors: kronenberg f.
PLoS One. 2012;7(4):e35015. doi: 10.1371/journal.pone.0035015. Epub 2012 Apr 11.
PLoS One. 2012.
PMID: 22509377
Free PMC article.