Genotype–Phenotype Characteristics of Children with Distal Renal Tubular Acidosis Caused by WDR72 Mutations: A Systematic Review of Case Reports-Reference-Cited by-同舟云学术

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Genotype–Phenotype Characteristics of Children with Distal Renal Tubular Acidosis Caused by WDR72 Mutations: A Systematic Review of Case Reports

Published:2023 Issue:2 Volume:3 Page:117
ISSN:2772-5170
Container-title:Indian Pediatrics Case Reports
language:en
Short-container-title:Indian Pediatr Case Rep

Author:

Bhatt GirishChandra,Todkar Mugdha,Harshitha S

Publisher

Medknow

Reference15 articles.

1. Treatment and long-term outcome in primary distal renal tubular acidosis;Lopez-Garcia;Nephrol Dial Transplant,2019

2. Hypokalemic distal renal tubular acidosis;Vallés;Adv Chronic Kidney Dis,2018

3. When to suspect a genetic disorder in a patient with renal stones, and why;Ferraro;Nephrol Dial Transplant,2013

4. Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations;Rungroj;Clin Genet,2018

5. Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta;El-Sayed;Am J Hum Genet,2009

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1. Oral Diseases as a Manifestation of Inborn Errors of Immunity;Journal of Clinical Medicine;2024-08-27

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