FRI283 Fragile X Gene Mutations Alter GnRH Neuron And Ovarian Innervation With Consequences On Reproductive Function

Disclosure: P.A. Villa: None. N. Lainez: None. C.R. Jonak: None. S. Berlin: None. I. Ethell: None. D. Coss: None. Mutations in the Fragile X messenger ribonucleoprotein 1 gene (FMR1) cause Fragile X syndrome, the most common cause of inherited mental disability, attributed to the loss of the Fragile...

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Detalles Bibliográficos
Autores principales: Villa, Pedro A, Lainez, Nancy, Jonak, Carrie R, Berlin, Sarah, Ethell, Iryna, Coss, Djurdjica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Neuroendocrinology & Pituitary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553894/
http://dx.doi.org/10.1210/jendso/bvad114.1218

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