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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