Open AccessSAT-287 Hypogonadotropic Hypogonadism in RPL10 Mutation-Associated Syndromic Intellectual Disability
Author(s) -
Julia Broussard,
Figen Ugrasbul-Eksinar
Publication year - 2019
Publication title -
journal of the endocrine society
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.046
H-Index - 20
ISSN - 2472-1972
DOI - 10.1210/js.2019-sat-287
Subject(s) - hypogonadotropic hypogonadism , short stature , intellectual disability , missense mutation , microcephaly , genetics , hypotonia , medicine , biology , pediatrics , mutation , endocrinology , gene , hormone