Hassan Y. Naim

Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.

R. Jacob, K. Zimmer, H. Naim, 2000, The Journal of clinical investigation.

Induction of lactase biosynthesis in the human intestinal epithelial cell line Caco-2.

H. Hauri, H. Naim, B. Sander, 1994, European journal of biochemistry.

A mutation in a highly conserved region in brush-border sucrase-isomaltase and lysosomal alpha-glucosidase results in Golgi retention.

H. Hauri, J. Fransen, H. Naim, 1997, Journal of cell science.

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.

J. Fransen, H. Naim, C. P. Hollenberg, 1996, The Journal of clinical investigation.

Molecular pathogenicity of novel sucrase-isomaltase mutations found in congenital sucrase-isomaltase deficiency patients.

M. Amiri, Birthe Gericke, Hassan Y. Naim, 2017, Biochimica et biophysica acta. Molecular basis of disease.