Mutation of the MECP2 gene, the main cause of Rett syndrome, alters pubertal development and sex hormones in mice
A research team including personnel from the Departament of Biologia Celullar i Biologia Funcional at the Universitat of València (UV), the Unitat Predepartamental de Medicina at Universitat Jaume I of Castelló (UJI) and Queen Mary University of London (QMUL) has shown that a mutation in the Mecp2 g
<p>A research team including personnel from the Departament of Biologia Celullar i Biologia Funcional at the Universitat of València (UV), the Unitat Predepartamental de Medicina at Universitat Jaume I of Castelló (UJI) and Queen Mary University of London (QMUL) has shown that a mutation in the Mecp2 g</p>