Genotype–Phenotype Analysis in Pediatric Patients with Distal Renal Tubular Acidosis
Article 2018 en
Authors
EP
Eujin Park
MC
Myung Hyun Cho
HH
Hye Sun Hyun
Abstract
1 min read
SLC4A1 is the most common defective gene in Korean children with dRTA. Patients with SLC4A1 mutations show later onset and milder disease severity. Long-term follow-up of hearing ability, renal function, and growth is necessary for patients with dRTA.
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