Article
Biochemical analyses and molecular modeling explain the functional loss of 17β-hydroxysteroid dehydrogenase 3 mutant G133R in three Tunisian patients with 46, XY Disorders of Sex Development.
The Journal of steroid biochemistry and molecular biology - 1 Jan 2016
Engeli Roger T, Rhouma Bochra Ben, Sager Christoph P, Tsachaki Maria, Birk Julia, Fakhfakh Faiza, Keskes Leila, Belguith Neila, Odermatt Alex
Abstract excerpt
Mutations in the HSD17B3 gene resulting in 17β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) deficiency cause 46, XY Disorders of Sex Development (46, XY DSD). Approximately 40 different mutations in HSD17B3 have been reported; only few mutant enzymes have been mechanistically investigated. Here, we report novel compound heterozygous mutations in HSD17B3, composed of the nonsense mutation C206X and the missense...
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