Cubilin P1297L mutation associated with hereditary...

Blood 2000 / 07 Vol. 96; Iss. 2

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

Kristiansen, Mette, Aminoff, Maria, Jacobsen, Christian, de la Chapelle, Albert, Krahe, Ralf, Verroust, Pierre J., Moestrup, Søren K.
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Volume:
96
Journal:
Blood
DOI:
10.1182/blood.v96.2.405
Date:
July, 2000
File:
PDF, 183 KB
2000
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