Cargando…

Altered GnRH neuron and ovarian innervation characterize reproductive dysfunction linked to the Fragile X messenger ribonucleoprotein (Fmr1) gene mutation

INTRODUCTION: Mutations in the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene cause Fragile X Syndrome, the most common monogenic cause of intellectual disability. Mutations of FMR1 are also associated with reproductive disorders, such as early cessation of reproductive function in females. Whi...

Descripción completa

Detalles Bibliográficos
Autores principales: Villa, Pedro A., Lainez, Nancy M., Jonak, Carrie R., Berlin, Sarah C., Ethell, Iryna M., Coss, Djurdjica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9992745/
https://www.ncbi.nlm.nih.gov/pubmed/36909303
http://dx.doi.org/10.3389/fendo.2023.1129534