New PAX2 heterozygous mutation in a child with chronic kidney disease: a case report and review of the literature
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://link.springer.com/content/pdf/10.1186/s12882-018-1044-9.pdf
Reference31 articles.
1. Pirojsakul K, Mathews N, Seikaly MG. Chronic kidney disease in children: recent update. Open Urol Nephrol J. 2015;8(1):117–23.
2. Chadha V, Warady BA. Epidemiology of pediatric chronic kidney disease. Adv Chronic Kidney Dis. 2005;12(4):343–52.
3. Woolf AS, Winyard PJ. Gene expression and cell turnover in human renal dysplasia. Histol Histopathol. 2000;15(1):159–66.
4. Aguilar A. Development: Pax2 keeps nephron progenitors on track. Nat Rev Nephrol. 2017;13(8):444.
5. Warady BA, Chadha V. Chronic kidney disease in children: the global perspective. Pediatr Nephrol. 2007;22(12):1999.
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2. PAX2 Gene Mutation in Pediatric Renal Disorders—A Narrative Review;International Journal of Molecular Sciences;2023-08-13
3. Detection of De Novo PAX2 Variants and Phenotypes in Chinese Population: A Single-Center Study;Frontiers in Genetics;2022-03-31
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5. A novel PAX2 heterozygous mutation in a family with Papillorenal syndrome: A case report and review of the literature;American Journal of Ophthalmology Case Reports;2021-06
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