Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1

BACKGROUND AND OBJECTIVES: The Wilms tumor suppressor gene 1 (WT1) plays an essential role in urogenital and kidney development. Genotype/phenotype correlations of WT1 mutations with renal function and proteinuria have been observed in world-wide cohorts with nephrotic syndrome or Wilms tumor (WT)....

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Detalhes bibliográficos
Publicado no:Clin J Am Soc Nephrol
Main Authors: Lehnhardt, Anja, Karnatz, Claartje, Ahlenstiel-Grunow, Thurid, Benz, Kerstin, Benz, Marcus R., Budde, Klemens, Büscher, Anja K., Fehr, Thomas, Feldkötter, Markus, Graf, Norbert, Höcker, Britta, Jungraithmayr, Therese, Klaus, Günter, Koehler, Birgit, Konrad, Martin, Kranz, Birgitta, Montoya, Carmen R., Müller, Dominik, Neuhaus, Thomas J., Oh, Jun, Pape, Lars, Pohl, Martin, Royer-Pokora, Brigitte, Querfeld, Uwe, Schneppenheim, Reinhard, Staude, Hagen, Spartà, Giuseppina, Timmermann, Kirsten, Wilkening, Frauke, Wygoda, Simone, Bergmann, Carsten, Kemper, Markus J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2015
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4422247/
https://ncbi.nlm.nih.gov/pubmed/25818337
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2215/CJN.10141014
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