Transport to cell surface of intestinal sucrase-isomaltase is blocked in the Golgi apparatus in a patient with congenital sucrase-isomaltase deficiency.

Lignende værker

• Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.
  af: Naim, H Y, et al.
  Udgivet: (1988)
• Congenital sucrase-isomaltase deficiency. Identification of a glutamine to proline substitution that leads to a transport block of sucrase-isomaltase in a pre-Golgi compartment.
  af: Ouwendijk, J, et al.
  Udgivet: (1996)
• Congenital sucrase–isomaltase deficiency: A case report
  af: Rita Santos-Silva, et al.
  Udgivet: (2014-11-01)
• Congenital Sucrase-Isomaltase Deficiency: Summary of an Evaluation in One Family
  af: Chumpitazi, Bruno P., et al.
  Udgivet: (2012)
• The patient journey to diagnosis and treatment of congenital sucrase-isomaltase deficiency
  af: Smith, Heather, et al.
  Udgivet: (2021)