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A recurrent, de novo nonsense mutation in the GRIN2B gene, comparison of the clinical phenotypes

M. J. V. Hoffer, E. A. R. Nibbeling,T. T. Koopmann, S. Bollen, M. E. Y. Laurense-Bik, I. J. H. van Minderhout,J. Knijnenburg, N. Lamziera, M. Verschuren,I. F. A. Fokkema,A. van Haeringen,T. P. Potjer,C. A. L. Ruivenkamp,N. S. den Hollander

EUROPEAN JOURNAL OF HUMAN GENETICS（2018）

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