Clinical Aspects and Treatment of Congenital Sucrase-Isomaltase Deficiency
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Gastroenterology,Pediatrics, Perinatology and Child Health
Reference46 articles.
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2. Congenital sucrase-isomaltase deficiency.;Treem;J Pediatr Gastroenterol Nutr,1995
3. Sequence of the complete cDNA and the 5 structure of the human sucrase-isomaltase gene. Possible homology with a yeast glucoamylase.;Chantret;Biochem J,1992
4. Four mutations in the SI gene are responsible for the majority of clinical symptoms of CSID.;Uhrich;J Pediatr Gastroenterol Nutr,2012
5. Compound heterozygous mutations affect protein folding and function in patients with congenital sucrase-isomaltase deficiency.;Alfalah;Gastroenterology,2009
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