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Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy.

Bibliographic reference Moortgat, Stéphanie ; Désir, Julie ; Benoit, Valérie ; Boulanger, Sébastien ; Pendeville, Hélène ; et. al. Two novel EIF2S3 mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy.. In: American Journal of Medical Genetics. Part A, Vol. 170, no.11, p. 2927-2933 (2016)
Permanent URL http://hdl.handle.net/2078.1/184941
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