Late onset of Imerslund-Gräsbeck syndrome without proteinuria in four children of one family from the Lebanon
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[1] A. Dautry‐Varsat,et al. Megalin-dependent cubilin-mediated endocytosis is a major pathway for the apical uptake of transferrin in polarized epithelia , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[2] S. Moestrup,et al. Megalin- and cubilin-mediated endocytosis of protein-bound vitamins, lipids, and hormones in polarized epithelia. , 2001, Annual review of nutrition.
[3] H Birn,et al. Megalin and cubilin: synergistic endocytic receptors in renal proximal tubule. , 2001, American journal of physiology. Renal physiology.
[4] A. Chapelle,et al. Mutations in CUBN, encoding the intrinsic factor-vitamin B 12 receptor, cubilin, cause hereditary megaloblastic anaemia 1 , 1999, Nature Genetics.
[5] M. Çetin,et al. Familial selective vitamin B12 malabsorption (Imerslund-Gräsbeck syndrome) in a pool of Turkish patients. , 1995, Pediatric hematology and oncology.
[6] J. Walker-Smith,et al. Absent ileal uptake of IF-bound vitamin B12 in vivo in the Imerslund-Grasbeck syndrome (familial vitamin B12 malabsorption with proteinuria). , 1985, Gut.