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1.3.1.22
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mutations of the SRD5A2 gene, e.g. Leu55Gln, cause 5alpha-reductase type 2 deficiency and masculinization defects of varying degree as a result of a prenatal lack of 5alpha-dihydrotestosterone to predominantly female phenotype newborn patient, detailed overview
712125
1.3.1.22
physiological function
conversion of testosterone to 5alpha-dihydrotestosterone is essential for correct development of genetalia, overview
712125
1.3.1.22
physiological function
SRD5A2 and dihydrotestosterone play important roles in benign prostatic hyperplasia
713595
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