SLC26A3 mutation in Turkish neonate and her sibling with congenital chloride diarrhea
{{output}}
Congenital chloride diarrhea is a rare cause of severe infantile diarrhea with excessive chloride excretion. Mutations in the SLC26A3 gene cause congenital chloride diarrhea. It generally becomes apparent in the neonatal period and is characterized by electrol... ...
