Expanding the phenotypic spectrum associated with OPHN1 mutations: Report of 17 individuals with intellectual disability but no cerebellar hypoplasia
- Resource Type
- Review Article
- Authors
- Moortgat, Stéphanie; Lederer, Damien; Deprez, Marie; Buzatu, Marga; Clapuyt, Philippe; Boulanger, Sébastien; Benoit, Valérie; Mary, Sandrine; Guichet, Agnès; Ziegler, Alban; Colin, Estelle; Bonneau, Dominique; Maystadt, Isabelle
- Source
- In European Journal of Medical Genetics August 2018 61(8):442-450
- Subject
- Language
- ISSN
- 1769-7212