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Article

Autosomal recessive distal renal tubular acidosis associated with Southeast Asian ovalocytosis.

Kidney international - 1 Nov 1999

Vasuvattakul S, Yenchitsomanus P T, Vachuanichsanong P, Thuwajit P, Kaitwatcharachai C, Laosombat V, Malasit P, Wilairat P, Nimmannit S

Abstract excerpt

BACKGROUND: A defect in the anion exchanger 1 (AE1) of the basolateral membrane of type A intercalated cells in the renal collecting duct may result in a failure to maintain a cell-to-lumen H+ gradient, leading to distal renal tubular acidosis (dRTA). Thus, dRTA may occur in Southeast Asian ovalocytosis (SAO), a common AE1 gene abnormality observed in Southeast Asia and Melanesia. Our study investigated whether...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10571775
DOI: 10.1046/j.1523-1755.1999.00756.x

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Autosomal recessive distal renal tubular acidosis associated with Southeast Asian ovalocytosis.PMID 10571775Read ↗

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Band 3 mutations, distal renal tubular acidosis, and Southeast Asian ovalocytosis.Semantic proximity Read ↗

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Trafficking defect of mutant kidney anion exchanger 1 (kAE1) proteins associated with distal renal tubular acidosis and Southeast Asian ovalocytosis.Semantic proximity Read ↗

Autosomal dominant distal renal tubular acidosis is associated in three families with heterozygosity for the R589H mutation in the AE1 (band 3) Cl-/HCO3- exchanger.Semantic proximity Read ↗

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