Related references
Note: Only part of the references are listed.Clinical perspectives in congenital adrenal hyperplasia due to 3-hydroxysteroid dehydrogenase type 2 deficiency
Abdullah M. Al Alawi et al.
ENDOCRINE (2019)
Mutational analysis of rare subtypes of congenital adrenal hyperplasia in a highly inbred population
Meshael M. Alswailem et al.
MOLECULAR AND CELLULAR ENDOCRINOLOGY (2018)
Human 3beta-hydroxysteroid dehydrogenase deficiency associated with normal spermatic numeration despite a severe enzyme deficit
Bruno Donadille et al.
ENDOCRINE CONNECTIONS (2018)
Testicular Adrenal Rest Tumor in Two Brothers with a Novel Mutation in the 3-Beta-Hydroxysteroid Dehydrogenase-2 Gene
Ayla Guven et al.
JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY (2017)
In silico structural, functional and pathogenicity evaluation of a novel mutation: An overview of HSD3B2 gene mutations
Bahareh Rabbani et al.
GENE (2012)
Carboxyl-terminal mutations in 3 beta-hydroxysteroid dehydrogenase type II cause severe salt-wasting congenital adrenal hyperplasia
Maik Welzel et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2008)
Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3β-hydroxysteroid dehydrogenase deficiency
TH Johannsen et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)
Refining hormonal diagnosis of type II 3β-hydroxysteroid dehydrogenase deficiency in patients with premature pubarche and hirsutism based on HSD3B2 genotyping
LM Mermejo et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2005)