Genotype–Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis
Background/Aims: Primary distal renal tubular acidosis (dRTA) in children is a rare genetic disorder, and three causative mutated genes have been identified: SLC4A1, ATP6V1B1, and ATP6V0A4. We analyzed the prevalence and phenotypic differences of genetic mutations in children with dRTA. Methods: A t...
Main Authors: | , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Karger Publishers
2018-03-01
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Series: | Kidney & Blood Pressure Research |
Subjects: | |
Online Access: | https://www.karger.com/Article/FullText/488698 |