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Navigating MARRVEL, a Web-Based Tool that Integrates Human Genomics and Model Organism Genetics Information
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The earlier described mutation (c.307c > T [p.R103X]) in the SRD5A2 gene causing a 46,XY female phenotype

Enver Simsek1, Cigdem Binay, Serdar Ceylaner

  • 1Department of Pediatric Endocrinology, School of Medicine, Eskisehir Osmangazi University, Eskisehir, Turkey. enversimsek06@hotmail.com

Journal of Pediatric Endocrinology & Metabolism : JPEM
|August 11, 2012
PubMed

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