Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II.

Autor: Hassan, Heba Amin, Mazen, Inas, Elaidy, Aya, Kamel, Alaa K, Eissa, Noura R., Essawi, Mona L.
Zdroj: Hormones; Jun2024, Vol. 23 Issue 2, p305-312, 8p
Databáze: Complementary Index