Genotype–Phenotype Correlation Analysis and Identification of a Novel SRD5A2 Mutation in Four Unrelated Chinese Patients with 5α-Reductase Deficiency
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Reference30 articles.
1. Steroid 5α-Reductase Deficiency in Man: An Inherited Form of Male Pseudohermaphroditism
2. Familial Incomplete Male Pseudohermaphroditism, Type 2
3. Androgens and male physiology the syndrome of 5α-reductase-2 deficiency
4. New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype–phenotype profiling of SRD5A2 in 190 Chinese patients
5. Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency Worldwide
Integrative and Analytical Review of the 5-Alpha-Reductase Type 2 Deficiency Worldwide
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