Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and CUBN[original query] |
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Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. The Journal of clinical investigation 2019 10 130 (1): 335-344. Bedin Mathilda, Boyer Olivia, Servais Aude, Li Yong, Villoing-Gaudé Laure, Tête Marie-Josephe, Cambier Alexandra, Hogan Julien, Baudouin Veronique, Krid Saoussen, Bensman Albert, Lammens Florie, Louillet Ferielle, Ranchin Bruno, Vigneau Cecile, Bouteau Iseline, Isnard-Bagnis Corinne, Mache Christoph J, Schäfer Tobias, Pape Lars, Gödel Markus, Huber Tobias B, Benz Marcus, Klaus Günter, Hansen Matthias, Latta Kay, Gribouval Olivier, Morinière Vincent, Tournant Carole, Grohmann Maik, Kuhn Elisa, Wagner Timo, Bole-Feysot Christine, Jabot-Hanin Fabienne, Nitschké Patrick, Ahluwalia Tarunveer S, Köttgen Anna, Andersen Christian Brix Folsted, Bergmann Carsten, Antignac Corinne, Simons Mati |
Molecular Genetic Testing for Kidney Disorders During the COVID-19 Pandemic. Delaware journal of public health 2022 5 7 (5): 24-27. Kirwin Susan M, Robbins Katherine M, Vinette Kathleen M B, Hirata Lee, Gripp Karen W, Funanage Vicky |
Polymorphisms in LRP2 and CUBN genes and their association with serum vitamin D levels and sleep apnea. Sleep & breathing = Schlaf & Atmung 2023 11 . Dimitra Anatolou, Paschalis Steiropoulos, Athanasios Zissimopoulos, Konstantina Chadia, Kostas Archontogeorgis, George Kolios, Vangelis G Manolopoulos, Georgia Rag |
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- Page last updated:May 06, 2024
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