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2. Hepcidin-Mediated Hypoferremia Disrupts Immune Responses to Vaccination and Infection

3. Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice

4. A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia

10. Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9

11. Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

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