Canine Imerslund-Gräsbeck syndrome maps to a region orthologous to HSA14q

  title={Canine Imerslund-Gr{\"a}sbeck syndrome maps to a region orthologous to HSA14q},
  author={Qianchuan He and John C. Fyfe and Alejandro A. Sch{\"a}ffer and Adam Kilkenney and Petra Werner and Ewen F. Kirkness and Paula S. Henthorn},
  journal={Mammalian Genome},
Selective malabsorption of cobalamin (vitamin B12) accompanied by proteinuria, known as Imerslund-Gräsbeck syndrome or megaloblastic anemia 1 (I-GS, MGA1; OMIM 261100), is a rare autosomal recessive disorder. In Finnish kindreds, I-GS is caused by mutations in the cubilin gene (CUBN), located on human Chromosome (Chr) 10. However, not all patients have CUBN mutations, and three distinct mutations in the amnionless gene, AMN, were very recently identified in patients from Norwegian and Israeli… CONTINUE READING
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