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Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1.
Münch, Johannes; Kirschner, Karin M; Schlee, Hendrik; Kraus, Cornelia; Schönauer, Ria; Jin, Wenjun; Le Duc, Diana; Scholz, Holger; Halbritter, Jan.
Affiliation
  • Münch J; Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Saxony, Germany.
  • Kirschner KM; Institute of Vegetative Physiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Berlin, Germany.
  • Schlee H; Dialysis Weissenfels, Nephrology Burgenlandkreis, Weissenfels, Germany.
  • Kraus C; Institute of Human Genetics, Friedrich-Alexander-University Erlangen-Nuremberg, Erlangen, Germany.
  • Schönauer R; Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Saxony, Germany.
  • Jin W; Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Saxony, Germany.
  • Le Duc D; Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Saxony, Germany.
  • Scholz H; Institute of Vegetative Physiology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Berlin, Germany.
  • Halbritter J; Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig Medical Center, Leipzig, Saxony, Germany jan.halbritter@medizin.uni-leipzig.de.
J Med Genet ; 2020 May 07.
Article in En | MEDLINE | ID: mdl-32381729
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Med Genet Year: 2020 Document type: Article Affiliation country: Country of publication:
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: J Med Genet Year: 2020 Document type: Article Affiliation country: Country of publication: