Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
Maria Aminoff(Cancer Genetics (United States)), Jo Ellen Carter(Cancer Genetics (United States)), Robert B. Chadwick(Cancer Genetics (United States)), Cheryl K.H. Johnson(Cancer Genetics (United States)), Ralph Gräsbeck(Minerva Foundation), Mohamed Abdelaal, Harald Broch(Sykehuset i Vestfold), L. Jenner(Aarhus University), P Verroust(Inserm), Søren K. Moestrup(Aarhus University), Albert de la Chapelle(University of Helsinki), Ralf Krahe(University of Helsinki)
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