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Genotype Is Associated to the Degree of Virilization in Patients With Classic Congenital Adrenal Hyperplasia

Background: Molecular defects of CYP21A2 consistently decrease 21-hydroxylase activity and result in a variable expression of disease severity in patients with congenital adrenal hyperplasia (CAH). Aim: The genotype and biochemical findings were examined in an attempt to reveal any association to th...

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Detalles Bibliográficos
Autores principales:	Neocleous, Vassos, Fanis, Pavlos, Phylactou, Leonidas A., Skordis, Nicos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2018
Materias:	Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6286958/ https://www.ncbi.nlm.nih.gov/pubmed/30559721 http://dx.doi.org/10.3389/fendo.2018.00733

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