1 diciembre 2014
The cause for a disorder common in Inuit people that prevents the absorption of sucrose, causing gastrointestinal distress and failure to thrive in infants, has been discovered by researchers. The study identified a genetic mutation responsible for the disorder, called congenital sucrose-isomaltase deficiency.
http://feeds.sciencedaily.com/~r/sciencedaily/~3/bIlg6pzQAVQ/141201125150.htm
