Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations

Gil Chernin, Virginia Vega-Warner, Dominik S. Schoeb, Saskia F. Heeringa, Bugsu Ovunc, Pawaree Saisawat, Roxana Cleper, Fatih Ozaltin, Friedhelm Hildebrandt*, A. Arbeiter, A. Bakkalogulu, M. Benz, D. Bockenhauer, R. Bogdanovic, V. Chandha, R. Ettenger, C. Ghossein, A. Goldberg, J. Heiliczer, D. HooperB. Hoppe, R. Jenkins, B. Kaplan, M. J. Kemper, M. Konrad, R. London, C. Mache, O. Mansoor, M. Mayr, T. Neuhaus, C. Plank, G. Reusz, C. Rinat, T. Seeman, M. Strecker, K. Taranta-Janusz, F. Weigel, A. Zolotnitskaya

*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

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Medicine and Dentistry

Biochemistry, Genetics and Molecular Biology