Imerslund-Gräsbeck syndrome: new mutation in amnionless

Pediatr Int. 2012 Jun;54(3):e19-21. doi: 10.1111/j.1442-200X.2011.03482.x.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Anemia, Megaloblastic
  • Child, Preschool
  • Humans
  • Malabsorption Syndromes / genetics*
  • Male
  • Membrane Proteins
  • Mutation*
  • Proteins / genetics*
  • Proteinuria / genetics*
  • Vitamin B 12 Deficiency / genetics*

Substances

  • AMN protein, human
  • Membrane Proteins
  • Proteins

Supplementary concepts

  • Imerslund-Grasbeck syndrome