A partial loss-of-function variant in GNRNR gene in a Chinese cohort with idiopathic hypogonadotropic hypogonadism

BACKGROUND: Idiopathic hypogonadotropic hypogonadism (IHH) is a rare genetic disease attributed to the disorder of hypothalamic-pituitary-gonadal axis. Mutations in the GNRHR gene are one of the most common genetic causes of IHH. Herein, we aimed to investigate GNRHR variants in a Chinese cohort wit...

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Detalles Bibliográficos
Autores principales: Chen, Yinwei, Sun, Taotao, Niu, Yonghua, Wang, Daoqi, Liu, Kang, Wang, Tao, Wang, Shaogang, Xu, Hao, Liu, Jihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100836/
https://www.ncbi.nlm.nih.gov/pubmed/33968656
http://dx.doi.org/10.21037/tau-20-1390

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8100836/
https://www.ncbi.nlm.nih.gov/pubmed/33968656
http://dx.doi.org/10.21037/tau-20-1390

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