Implication of Heterozygous Variants in PROX1 in Congenital Anomalies of the Kidneys and Urinary Tract: TH-OR85
Kolvenbach, Caroline Maria, Merz, Lea Maria, Aslam, Faiza, Sanna-Cherchi, Simone, Milo Rasouly, Hila, Gharavi, Ali G., Pena, Sergio D.j., Tasic, Velibor, Li, Zhongwei, Shril, Shirlee, Hildebrandt, Friedhelm
Published in Journal of the American Society of Nephrology (01.10.2024)
Published in Journal of the American Society of Nephrology (01.10.2024)
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Adeno-Associated Virus (AAV)-Mediated Gene Therapy in Nphs1 Knockout Mice: A Strategy for Treating Congenital Nephrotic Syndrome: SA-PO642
Saida, Ken, Yu, Seyoung, Braun, Alina, Franken, Gijs AC, Lomjansook, Kraisoon, Lemberg, Katharina, Kolvenbach, Caroline Maria, Mansour, Bshara, Yousef, Kirollos, Riedhammer, Korbinian M., Mertens, Nils David, Elmubarak, Izzeldin, Schneider, Ronen, Shril, Shirlee, Buerger, Florian, Hildebrandt, Friedhelm
Published in Journal of the American Society of Nephrology (01.10.2024)
Published in Journal of the American Society of Nephrology (01.10.2024)
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Exome Sequencing Reveals a Monogenic Cause of Kidney Disease in 34% of Pediatric Patients at a Single Saudi Arabian Center: FR-PO654
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Published in Journal of the American Society of Nephrology (01.10.2024)
Published in Journal of the American Society of Nephrology (01.10.2024)
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