Two novelEIF2S3mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy-Reference-Cited by-同舟云学术

Two novelEIF2S3mutations associated with syndromic intellectual disability with severe microcephaly, growth retardation, and epilepsy

Author:

Moortgat Stéphanie¹,Désir Julie²,Benoit Valérie¹,Boulanger Sébastien¹,Pendeville Hélène³,Nassogne Marie-Cécile⁴,Lederer Damien¹,Maystadt Isabelle¹

Affiliation:

1. Centre de Génétique Humaine; Institut de Pathologie et de Génétique; Charleroi (Gosselies) Belgium

2. Centre de Génétique Humaine; Hôpital Erasme; Université Libre de Bruxelles (ULB); Brussels Belgium

3. GIGA-Research; Zebrafish Platform, Tour B34; Université de Liège; Liège (Sart-Tilman) Belgium

4. Département de Neuropédiatrie; Cliniques Universitaires Saint-Luc; Brussels Belgium

Funder

Institut de Recherche Scientifique en Pathologie et Génétique

Fonds Marguerite-Marie Delacroix

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference19 articles.

5. 2015

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