bibliographic entry 9201787 [be/9201787]
https://w3id.org/oc/corpus/be/9201787
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Aminoff, M, Carter, JE, Chadwick, RB, Johnson, C, Grasbeck, R, Abdelaal, MA, Broch, H, Jenner, LB, Verroust, PJ, Moestrup, SK. 1999 Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nat Genet. 21: 309â313. PMID: 10080186
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