Molecular analysis of 5α-reductase type 2 gene in eight unrelated egyptian children with suspected 5α-reductase deficiency: prevalence of the G34R mutation
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.2003.01763.x/fullpdf
Reference23 articles.
1. Familial male pseudohermaphroditism due to 5-α-reductase deficiency in a Turkish village;Akgun;American Journal of Medicine,1986
2. Deletion of steroid 5-α-reductase 2 gene in male pseudohermaphroditism;Andersson;Nature,1991
3. Genotype versus phenotype in families with androgen insensitivity syndrome;Boehmer;Journal of Clinical Endocrinology and Metabolism,2001
4. Molecular study of the 5-α-reductase type 2 gene in three European families with 5-α-reductase deficiency;Boudon;Journal of Clinical Endocrinology and Metabolism,1995
5. Mutations of the 5-α-reductase type 2 gene in eight Mexican patients from six different pedigrees with 5-α-reductase-2 deficiency;Canto;Clinical Endocrinology,1997
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