Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF

Παρόμοια τεκμήρια

• Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene
  ανά: Tanner, Stephan M., κ.ά.
  Έκδοση: (2005)
• Evidence for a BRCA1 founder mutation in families of West African ancestry.
  ανά: Mefford, H C, κ.ά.
  Έκδοση: (1999)
• Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
  ανά: Tanner Stephan M, κ.ά.
  Έκδοση: (2012-08-01)
• Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns
  ανά: Tanner, Stephan M, κ.ά.
  Έκδοση: (2012)
• Juvenile Cobalamin Deficiency in a 17 Year Old Child with Autonomic Dysfunction and Skin Changes
  ανά: Siddiqui, Abdul Hafeez, κ.ά.
  Έκδοση: (2012)