New NR5A1 mutations and phenotypic variations of gonadal dysgenesis

Mutations in NR5A1 have been reported as a frequent cause of 46,XY disorders of sex development (DSD) associated to a broad phenotypic spectrum ranging from infertility, ambiguous genitalia, anorchia to gonadal dygenesis and female genitalia. Here we present the clinical follow up of four 46,XY DSD...

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Detalles Bibliográficos
Autores principales: Werner, Ralf, Mönig, Isabel, Lünstedt, Ralf, Wünsch, Lutz, Thorns, Christoph, Reiz, Benedikt, Krause, Alexandra, Schwab, Karl Otfried, Binder, Gerhard, Holterhus, Paul-Martin, Hiort, Olaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411087/
https://www.ncbi.nlm.nih.gov/pubmed/28459839
http://dx.doi.org/10.1371/journal.pone.0176720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411087/
https://www.ncbi.nlm.nih.gov/pubmed/28459839
http://dx.doi.org/10.1371/journal.pone.0176720

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