Variations in the 3′UTR of the CYP21A2 Gene in Heterozygous Females with Hyperandrogenaemia

Heterozygosity for CYP21A2 mutations in females is possibly related to increased risk of developing clinical hyperandrogenism. The present study was designed to seek evidence on the phenotype-genotype correlation in female children, adolescents, and women with CYP21A2 mutations and variants in the 3...

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Detalles Bibliográficos
Autores principales: Neocleous, Vassos, Fanis, Pavlos, Toumba, Meropi, Phedonos, Alexia A. P., Picolos, Michalis, Andreou, Elena, Kyriakides, Tassos C., Tanteles, George A., Shammas, Christos, Phylactou, Leonidas A., Skordis, Nicos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405599/
https://www.ncbi.nlm.nih.gov/pubmed/28487735
http://dx.doi.org/10.1155/2017/8984365

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405599/
https://www.ncbi.nlm.nih.gov/pubmed/28487735
http://dx.doi.org/10.1155/2017/8984365

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