Congenital glucose-galactose malabsorption: A case report with a novel SLC5A1 mutation
Author:
Affiliation:
1. Department of Pediatrics, School of Medicine; The university of Jordan; Amman Jordan
2. Department of Pediatrics, College of Medicine; University of Iowa; Iowa City Iowa
Publisher
Wiley
Subject
General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ccr3.1913/fullpdf
Reference11 articles.
1. Analysis and update of the human solute carrier (SLC) gene superfamily;He;Human Genomics,2009
2. Congenital glucose-galactose malabsorption: A descriptive study of clinical characteristics and outcome from Western Saudi Arabia;Saadah;Arab J Gastroenterol,2014
3. Congenital diarrheal disorders: an updated diagnostic approach;Terrin;Int J Mol Sci,2012
4. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology;Richards;Genet Med,2015
5. Congenital glucose-galactose malabsorption in a Turkish Newborn: A novel mutation of Na /Glucose cotransporter gene;Atay;Dig Dis Sci,2016
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