Browsing by Subject "ATP6V1B1 protein, human"
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Article
Molecular investigation of distal renal tubular acidosis in Tunisia, evidence for founder mutations
(2014)BACKGROUND: Distal renal tubular acidosis (dRTA) is a rare genetic disease caused by mutations in different genes involved in the secretion of H+ ions in the intercalated cells of the collecting duct. Both autosomal dominant ...