Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1

Kallmann syndrome (KS) is a common type of idiopathic hypogonadotropic hypogonadism. To date, more than 30 genes including ANOS1 and FGFR1 have been identified in different genetic models of KS without affirmator...

Source: Reproductive Biology and Endocrinology - March 1, 2023 Category: Endocrinology Authors: Guoming Chu, Pingping Li, Qian Zhao, Rong He and Yanyan Zhao Tags: Research Source Type: research