Clinical and genetic analysis of distal renal tubular acidosis in three Chinese children
Author:
Affiliation:
1. Department of Nephrology, Children’s Hospital of Fudan University, Shanghai, China
Publisher
Informa UK Limited
Subject
Nephrology,Critical Care and Intensive Care Medicine,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/0886022X.2018.1487858
Reference30 articles.
1. Renal tubular acidosis
2. Inherited Distal Renal Tubular Acidosis
3. Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss
4. Confirmation of the ATP6B1 gene as responsible for distal renal tubular acidosis
5. Molecular investigation and long-term clinical progress in Greek Cypriot families with recessive distal renal tubular acidosis and sensorineural deafness due to mutations in the ATP6V1B1 gene
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2. Mutations and clinical characteristics of dRTA caused by SLC4A1 mutations: Analysis based on published patients;Frontiers in Pediatrics;2023-01-26
3. Hearing Loss Related to Gene Mutations in Distal Renal Tubular Acidosis;Audiology and Neurotology;2023
4. Molecular Aspects of Distal Kidney Tubular Acidosis in Children, Its Long-Term Outcome, and Relationship with Hyperammonemia;Turkish Archives of Pediatrics;2022-07-07
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