Associated Papers
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393W.
Reimold FR et al.
Frontiers in Physiology, 2015
Update on SLC26A3 mutations in congenital chloride diarrhea.
Wedenoja S et al.
Human Mutation, 2011
Significance of molecular testing for congenital chloride diarrhea.
Lechner S et al.
Journal of Pediatric Gastroenterology and Nutrition, 2011
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