Moortgat, S., Désir, J., Benoit, V., Boulanger, S., Pendeville, H., Nassogne, M.C., Lederer, D., Maystadt, I. (2016) Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. American journal of medical genetics. Part A. 170(11):2927-2933

Moortgat, S., Désir, J., Benoit, V., Boulanger, S., Pendeville, H., Nassogne, M.C., Lederer, D., Maystadt, I. (2016) Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy. American journal of medical genetics. Part A. 170(11):2927-2933