Author:
Ament Andrea E.,Li Zhongyuan,Sturm Amy C.,Perko James D.,Lawson Sarah,Masterson Margaret,Quadros Edward V.,Tanner Stephan M.
Reference10 articles.
1. Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1;Aminoff;Nature Genetics,1999
2. Update on cobalamin, folate, and homocysteine;Carmel;Hematology (American Society of Hematology Education Program),2003
3. Imerslund-Gräsbeck Syndrome (Selective Vitamin B12 Malabsorption with Proteinuria);Gräsbeck;Orphanet journal of rare diseases,2006
4. Selective vitamin B12 malabsorption and proteinuria in young people;Gräsbeck;Acta medica Scandinavica,1960
5. Idiopathic chronic megaloblastic anemia in children;Imerslund;Acta paediatrica Scandinavica,1960
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