Associated Papers
Rectal Cancer in a Patient with Bartter Syndrome: A Case Report.
Fujino S et al.
Genes, 2017
Congenital chloride-losing diarrhea in a Mexican child with the novel homozygous SLC26A3 mutation G393W.
Reimold FR et al.
Frontiers in Physiology, 2015
Extensive molecular analysis of patients bearing CFTR-related disorders.
Amato F et al.
The Journal of Molecular Diagnostics : Jmd, 2012
Update on SLC26A3 mutations in congenital chloride diarrhea.
Wedenoja S et al.
Human Mutation, 2011
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