Shaogang Wang

No ORCID on file · 2 papers in corpus
other 2022
Cell & bioscience ·doi:10.1186/s13578-022-00790-x

BACKGROUND: Von Hippel-Lindau (VHL) disease is an autosomal dominant genetic neoplastic disorder caused by germline mutation or deletion of the VHL gene, characterized by the tendency to develop multisystem benign or malignant tumors. The m…

other 2021
Translational andrology and urology ·doi:10.21037/tau-20-1390

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…