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Academic Journal

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

  • Authors : Kloss-Brandstätter A; Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Innsbruck, Austria.; Erhart G

Subjects: Haplotypes*; Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/*blood ; Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/Anemia, Iron-Deficiency/*genetics

  • Source: PloS one [PLoS One] 2012; Vol. 7 (4), pp. e35015. Date of Electronic Publication: 2012 Apr 11.Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: Print-Electronic Cited Medium: Internet

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