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. |
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Zdroj: | Hormones; Jun2024, Vol. 23 Issue 2, p305-312, 8p |
Databáze: | Complementary Index |
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