Updated insight into the mutational and phenotypic spectrum of MED13L-related intellectual disability

R. Asadollahi, P. Boonsawat, B. Popp, E. Torti, I. Bader, A. Vitobello, S. Moutton, L. Pinson, L. Lambert, A. C. Thuresson, M. Sobol, C. Soussi Zander, K. Platzer, V. Strehlow, F. Hornemann, P. Zacher, F. Tran Mau-Them, A. L. Bruel, M. J. Hajianpour, R. Kovacs-Nagy, G. Lay-Son, L. Amlie-Wolf, J. Kaplan, A. Chassevent, C. Smith-Hicks, A. Slavotinek, M. K. Kukolich, K. Nugent, E. Roeder, Y. A. Zarate, Y. Toshiyuki, C. Jackel-Cram, I. Maystadt, S. G. Mehta, T. A. Briggs, K. Chandler, A. van Haeringen, C. Kraus, C. Zweier, A. Reis, A. Rauch

EUROPEAN JOURNAL OF HUMAN GENETICS（2020）

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