Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B12 by cubilin

Blood

Volumn 96, Issue 2, 2000, Pages 405-409

  Kristiansen, Mette ^b   Aminoff, Maria ^b   Jacobsen, Christian ^b   De La Chapelle, Albert ^b   Krahe, Ralf ^b   Verroust, Pierre J ^b   Moestrup, Søren K ^a  

^a AARHUS UNIVERSITY   (Denmark)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

COBALAMIN DERIVATIVE; CYANOCOBALAMIN; INTRINSIC FACTOR;

ANEMIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BINDING SITE; EPITHELIUM CELL; GENE MUTATION; LIGAND BINDING; MALABSORPTION; MEGALOBLASTIC ANEMIA; PRIORITY JOURNAL; PROTEIN BINDING; SITE DIRECTED MUTAGENESIS; SURFACE PLASMON RESONANCE;

EID: 0034661941     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v96.2.405.014k16_405_409     Document Type: Article

References (20)

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