Degenerative Liver Disease in Young Beagles with Hereditary Cobalamin Malabsorption Because of a Mutation in the Cubilin Gene

Những quyển sách tương tự

• A Frameshift Mutation in the Cubilin Gene (CUBN) in Border Collies with Imerslund-Gräsbeck Syndrome (Selective Cobalamin Malabsorption)
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  Được phát hành: (2013)
• Daily oral cyanocobalamin supplementation in Beagles with hereditary cobalamin malabsorption (Imerslund‐Gräsbeck syndrome) maintains normal clinical and cellular cobalamin status
  Bằng: Kook, Peter H., et al.
  Được phát hành: (2018)
• Prospective long‐term evaluation of parenteral hydroxocobalamin supplementation in juvenile beagles with selective intestinal cobalamin malabsorption (Imerslund‐Gräsbeck syndrome)
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  Được phát hành: (2018)
• Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund‐Gräsbeck Syndrome) in Juvenile Beagles
  Bằng: Fyfe, J.C., et al.
  Được phát hành: (2014)
• Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
  Bằng: Tanner Stephan M, et al.
  Được phát hành: (2012-08-01)