EGAS00001002568

Study Description

Congenital hypogonadotropic hypogonadism (CHH) is a rare genetic form of isolated gonadotropin-releasing hormone (GnRH) deficiency caused by... Show More

EGAS00001002568

Study Accession Alternative Stable ID type
EGAS00001002568 Other

Publications

28754744

Who archives the data?

European Genome-phenome Archive