Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations

Graciana Jaureguiberry*, Muriel De La Dure-Molla, David Parry, Mickael Quentric, Nina Himmerkus, Toshiyasu Koike, James Poulter, Enriko Klootwijk, Steven L. Robinette, Alexander J. Howie, Vaksha Patel, Marie Lucile Figueres, Horia C. Stanescu, Naomi Issler, Jeremy K. Nicholson, Detlef Bockenhauer, Christopher Laing, Stephen B. Walsh, David A. McCredie, Sue PoveyAudrey Asselin, Arnaud Picard, Aurore Coulomb, Alan J. Medlar, Isabelle Bailleul-Forestier, Alain Verloes, Cedric Le Caignec, Gwenaelle Roussey, Julien Guiol, Bertrand Isidor, Clare Logan, Roger Shore, Colin Johnson, Christopher Inglehearn, Suhaila Al-Bahlani, Matthieu Schmittbuhl, François Clauss, Mathilde Huckert, Virginie Laugel, Emmanuelle Ginglinger, Sandra Pajarola, Giuseppina Spartà, Deborah Bartholdi, Anita Rauch, Marie Claude Addor, Paulo M. Yamaguti, Heloisa P. Safatle, Ana Carolina Acevedo, Hercílio Martelli-Júnior, Pedro E. Dos Santos Netos, Ricardo D. Coletta, Sandra Gruessel, Carolin Sandmann, Denise Ruehmann, Craig B. Langman, Steven J. Scheinman, Didem Ozdemir-Ozenen, Thomas C. Hart, P. Suzanne Hart, Ute Neugebauer, Eberhard Schlatter, Pascal Houillier, William A. Gahl, Miikka Vikkula, Agnès Bloch-Zupan, Markus Bleich, Hiroshi Kitagawa, Robert J. Unwin, Alan Mighell, Ariane Berdal, Robert Kleta

*Corresponding author for this work

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Medicine and Dentistry