المؤلفون: Kai-Uwe Eckardt, Eric Olinger, Stanislav Kmoch, Anthony J. Bleyer, Stefanie Weber, Luca Rampoldi, Olivier Devuyst

المساهمون: UCL - SSS/IREC/NEFR - Pôle de Néphrologie, UCL - (SLuc) Service de néphrologie, University of Zurich, Devuyst, Olivier, Devuyst, O, Olinger, E, Weber, S, Eckardt, Ku, Kmoch, S, Rampoldi, L, Bleyer, Aj

المصدر: Nature Reviews Disease Primers, Vol. 5, no. 1 (2019) (2019)

مصطلحات موضوعية: Kidney, business.industry, Biopsy, Autosomal dominant polycystic kidney disease, Genetic Diseases, Inborn, 610 Medicine & health, General Medicine, Disease, 2700 General Medicine, Interstitial fibrosis, medicine.disease, Bioinformatics, Polycystic kidney, HNF1B, Polycystic Kidney, Autosomal Dominant, 10052 Institute of Physiology, medicine.anatomical_structure, medicine, Humans, Kidney Failure, Chronic, 570 Life sciences, biology, Family history, business, Kidney disease

وصف الملف: Primer_s41572-019-0109-9_1567694997_1.pdf - application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::376c4dd2741634ca7a549840ab0e86ed
https://hdl.handle.net/2078.1/223677