Chandran Ka, Gérald Le Gac, Emilie Letocart, Isabelle Gourlaouen, Brigitte Martin, and Claude Férec. 2007. “Phenotypic and Functional Data Confirm Causality of the Recently Identified Hemojuvelin p.R176c Missense Mutation”. Haematologica 92 (9). Pavia, Italy, 1262-63. https://doi.org/10.3324/haematol.11247.