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CHD1L: A new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

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作者单位: Division of Pediatric Nephrology, University Children's Hospital, University of Heidelberg [1] Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany, Department of [2] KfH-Pediatric Kidney Center, Marburg, Germany [3] Division of Pediatric Nephrology, University Children's Hospital, Bern, Switzerland [4] Institute of Child Health, University College London, London, United Kingdom [5] Departamenti i Pediatrise Sherbimi i Nefrologjise, Qendra Spitalore Universitare Nene Tereza [6] Department of General Pediatrics, University Children's Hospital, Münster, Germany [7] Institute of Human Genetics, Rheinische Friedrich-Wilhelms-University, Bonn, Germany [8] Department of Pediatric Kidney., Liver and Metabolic Diseases, Hannover Medical School, Hannover [9]
发布时间 2013-11-20
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Nephrology, dialysis, transplantation: official publication of the European Dialysis and Transplant Association - European Renal Association

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