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Updated: Jun 22, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
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Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females

C Philippe1, D Amsallem, C Francannet

  • 1Laboratoire de Génétique Médicale, Nancy Université, EA 4002, Centre Hospitalier Régional et Universitaire, 54511 cedex 1, Vandoeuvre-les-Nancy, France. c.philippe@chu-nancy.fr

Journal of Medical Genetics
|July 1, 2009
PubMed
Abstract

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