Title : Japanese neonate with congenital chloride diarrhea caused by SLC26A3 mutation.

Pub. Date : 2015

PMID : 25711268






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Life-long secretory diarrhea is caused by mutations in solute carrier family 26, member 3, (SLC26A3), which disrupt epithelial Cl(-) /HCO3 (-) transport in the ileum and colon. Bicarbonates solute carrier family 26 member 3 Homo sapiens
2 Life-long secretory diarrhea is caused by mutations in solute carrier family 26, member 3, (SLC26A3), which disrupt epithelial Cl(-) /HCO3 (-) transport in the ileum and colon. Bicarbonates solute carrier family 26 member 3 Homo sapiens