Alfalah, Marwan

Up a level
Export as [feed] RSS
Group by: Item Type | No Grouping
Number of items: 2.

Alfalah, Marwan; Keiser, Markus; Leeb, Tosso; Zimmer, Klaus-Peter; Naim, Hassen Y. (2009). Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency. Gastroenterology, 136(3), pp. 883-892. Philadelphia, Pa.: Elsevier 10.1053/j.gastro.2008.11.038

Sander, Petra; Alfalah, Marwan; Keiser, Markus; Korponay-Szabo, Ilma; Kovács, Judit B; Leeb, Tosso; Naim, Hassan Y (2006). Novel mutations in the human sucrase-isomaltase gene (SI) that cause congenital carbohydrate malabsorption. Human mutation, 27(1), p. 119. Hoboken, N.J.: Wiley-Blackwell

This list was generated on Thu Mar 28 12:48:59 2024 CET.
Provide Feedback