Author(s): Rolfs、Arndt 教授醫學博士、Giese、Anne Katrin 醫學博士、Eichler、Sabrina 博士、Lukas Jan 博士、Kramp、Guido Johannes 博士、Mascher、Hermann 教授、Grittner、Ulrike 博士、Te Vruchte、Danielle、Al Eisa、Nada 博士、Cortina-Borja、Mbes
This is the first case report in Oman and the Gulf region of a 17-β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency with a novel mutation in the HSD17B3 gene that has not been previously described in the medical literature.
This is the first case report in Oman and the Gulf region of a 17-β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency with a novel mutation in the HSD17B3 gene that has not been previously described in the medical literature.