Discordant phenotypes in monozygotic twins with identical de novo WT1 mutation
Author:
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ckj/article-pdf/5/3/221/1186480/sfs030.pdf
Reference10 articles.
1. Denys-Drash Syndrome with Neonatal Renal Failure in Monozygotic Twins Due to C.1097G>A Mutation in the WT1 Gene
2. Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations
3. Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy
4. Genotype/Phenotype Correlation in Nephrotic Syndrome Caused byWT1Mutations
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy;Children;2023-03-17
2. DENYS–DRASH SYNDROME, FRASIER SYNDROME, AND WAGR SYNDROME ( WT1 ‐RELATED DISORDERS);Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30
3. Patients with different or identical genotypes of the WT1 gene present different phenotypes;European Journal of Pediatrics;2013-07-09
4. Wilms' tumor suppressor gene mutations in girls with sporadic isolated steroid-resistant nephrotic syndrome;Genetics and Molecular Research;2013
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