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by Mansour-Hendili, Lamisse and Blanchard, Anne and Le Pottier, Nelly and Roncelin, Isabelle and Lourdel, Stéphane and Treard, Cyrielle and González, Wendy and Vergara-Jaque, Ariela and Morin, Gilles and Colin, Estelle and Holder-Espinasse, Muriel and Bacchetta, Justine and Baudouin, Véronique and Benoit, Stéphane and Bérard, Etienne and Bourdat-Michel, Guylhène and Bouchireb, Karim and Burtey, Stéphane and Cailliez, Mathilde and Cardon, Gérard and Cartery, Claire and Champion, Gerard and Chauveau, Dominique and Cochat, Pierre and Dahan, Karin and De La Faille, Renaud and Debray, François-Guillaume and Dehoux, Laurenne and Deschenes, Georges and Desport, Estelle and Devuyst, Olivier and Dieguez, Stella and Emma, Francesco and Fischbach, Michel and Fouque, Denis and Fourcade, Jacques and François, Hélène and Gilbert-Dussardier, Brigitte and Hannedouche, Thierry and Houillier, Pascal and Izzedine, Hassan and Janner, Marco and Karras, Alexandre and Knebelmann, Bertrand and Lavocat, Marie-Pierre and Lemoine, Sandrine and Leroy, Valérie and Loirat, Chantal and Macher, Marie-Alice and Martin-Coignard, Dominique and Morin, Denis and Niaudet, Patrick and Nivet, Hubert and Nobili, François and Novo, Robert and Faivre, Laurence and Rigothier, Claire and Roussey-Kesler, Gwenaëlle and Salomon, Remi and Schleich, Andreas and Sellier-Leclerc, Anne-Laure and Soulami, Kenza and Tiple, Aurélien and Ulinski, Tim and Vanhille, Philippe and Van Regemorter, Nicole and Jeunemaître, Xavier and Vargas-Poussou, Rosa
Hum Mutat, ISSN 1098-1004, 2015, Volume 36, pp. 743 - 52
Dent disease is a rare X-linked tubulopathy characterized by low molecular weight proteinuria, hypercalciuria, nephrocalcinosis and/or nephrolithiasis,... 
Life Sciences | Human health and pathology
Journal Article
Molecular Vision, ISSN 1090-0535, 04/2007, Volume 13, Issue 52-55, pp. 511 - 523
Journal Article
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 06/2002, Volume 43, Issue 6, pp. 1715 - 1724
Journal Article
Human Mutation, ISSN 1059-7794, 10/2010, Volume 31, Issue 10, pp. E1709 - E1766
Journal Article
Nature Genetics, ISSN 1061-4036, 02/1997, Volume 15, Issue 2, pp. 157 - 164
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 07/2001, Volume 10, Issue 15, pp. 1591 - 1600
Journal Article
Human mutation, ISSN 1059-7794, 2008, Volume 29, Issue 11, pp. E205 - E219
Journal Article
by Mansour-Hendili, Lamisse and Blanchard, Anne and Le Pottier, Nelly and Roncelin, Isabelle and Lourdel, Stéphane and Treard, Cyrielle and González, Wendy and Vergara-Jaque, Ariela and Morin, Gilles and Colin, Estelle and Holder-Espinasse, Muriel and Bacchetta, Justine and Baudouin, Véronique and Benoit, Stéphane and Bérard, Etienne and Bourdat-Michel, Guylhène and Bouchireb, Karim and Burtey, Stéphane and Cailliez, Mathilde and Cardon, Gérard and Cartery, Claire and Champion, Gerard and Chauveau, Dominique and Cochat, Pierre and Dahan, Karin and De la Faille, Renaud and Debray, François-Guillaume and Dehoux, Laurenne and Deschenes, Georges and Desport, Estelle and Devuyst, Olivier and Dieguez, Stella and Emma, Francesco and Fischbach, Michel and Fouque, Denis and Fourcade, Jacques and François, Hélène and Gilbert-Dussardier, Brigitte and Hannedouche, Thierry and Houillier, Pascal and Izzedine, Hassan and Janner, Marco and Karras, Alexandre and Knebelmann, Bertrand and Lavocat, Marie-Pierre and Lemoine, Sandrine and Leroy, Valérie and Loirat, Chantal and Macher, Marie-Alice and Martin-Coignard, Dominique and Morin, Denis and Niaudet, Patrick and Nivet, Hubert and Nobili, François and Novo, Robert and Faivre, Laurence and Rigothier, Claire and Roussey-Kesler, Gwenaëlle and Salomon, Remi and Schleich, Andreas and Sellier-Leclerc, Anne-Laure and Soulami, Kenza and Tiple, Aurélien and Ulinski, Tim and Vanhille, Philippe and Van Regemorter, Nicole and Jeunemaître, Xavier and Vargas-Poussou, Rosa
Human Mutation, ISSN 1059-7794, 08/2015, Volume 36, Issue 8, pp. 743 - 752
Journal Article
Journal Article
Journal Article