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Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
The Lancet, 2012 A. Rauch, D. Wieczorek, E. Graf, T. Wieland, S. Endele, T. Schwarzmayr, B. Albrecht, D. Bartholdi, J. Beygo, N. Donato, A. Dufke, K. Cremer, M. Hempel, D. Horn, Juliane Hoyer, P. Joset, A. Röpke, U. Moog, A. Riess, C. Thiel, A. Tzschach, Antje Wiesener, E. Wohlleber, C. Zweier, A. Ekici, A. Zink, A. Rump, C. Meisinger, H. Grallert, H. Sticht, A. Schenck, H. Engels, G. Rappold, E. Schröck, P. Wieacker, O. Riess, T. Meitinger, A. Reis, T. Strom +38 moresemanticscholar +1 more source
