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...

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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:
Endocrinology
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

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