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European Journal of Pediatrics
Literature
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Benoit G, Machuca E, Antignac C (2010) Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations. Pediatr Nephrol 25:1621–1632
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Chernin G, Vega-Warner V, Schoeb DS, Heeringa SF, Ovunc B, Saisawat P, Cleper R, Ozaltin F, Hildebrandt F, Members of the GPN Study Group (2010) Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations. Clin J Am Soc Nephrol 5:1655–1662
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Fencl F, Malina M, Stará V, Zieg J, Mixová D, Seeman T, Bláhová K (2012) Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome. Eur J Pediatr 171:121–124PubMedCrossRef
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Hakan N, Aydin M, Erdogan O, Cavusoglu YH, Aycan Z, Ozaltin F, Zenciroglu A, Apaydin S, Gunes R, Sahin G, Cinar G, Okumus N (2012) A novel WT1 gene mutation in a newborn infant diagnosed with Denys–Drash syndrome. Genet Couns 23:255–261PubMed
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Takata A, Kikuchi H, Fukuzawa R, Ito S, Honda M, Hata J (2000) Constitutional WT1 mutations correlate with clinical features in children with progressive nephropathy. J Med Genet 37:698–701PubMedCrossRef
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Yang Y, Feng D, Huang J, Nie X, Yu Z (2013) A child with isolated nephrotic syndrome and WT1 mutation presenting as a 46, XY phenotypic male. Eur J Pediatr 172:127–129PubMedCrossRef
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Metadata
Title
Patients with different or identical genotypes of the WT1 gene present different phenotypes
Authors
Yonghui Yang
Feng Zhao
Jun Huang
Xiaojing Nie
Zihua Yu
Publication date
01-12-2013
Publisher
Springer Berlin Heidelberg
Published in
European Journal of Pediatrics / Issue 12/2013
Print ISSN: 0340-6199
Electronic ISSN: 1432-1076
DOI
https://doi.org/10.1007/s00431-013-2086-4

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