NPHS1 Gene Mutations in Children with Focal Segmental Glomerulosclerosis and Literature Review
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Published:2024
Issue:02
Volume:14
Page:3037-3044
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ISSN:2161-8712
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Container-title:Advances in Clinical Medicine
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language:
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Short-container-title:ACM
Publisher
Hans Publishers
Reference18 articles.
1. Genetic causes of focal segmental glomerulosclerosis: implications for clinical practice
2. New developments in steroid-resistant nephrotic syndrome
3. Genetics of Proteinuria: An Overview of Gene Mutations Associated with Nonsyndromic Proteinuric Glomerulopathies
4. 彭映潮, 高春林, 夏正坤. 儿童原发性局灶节段性肾小球硬化症治疗进展[J]. 临床儿科杂志, 2021, 39(8): 631-635.
5. Sadowski, C.E., Lovric, S., Ashraf, S., et al. (2015) A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome. Journal of the American Society of Nephrology, 26, 1279-1289.