Genotype-Phenotype Correlation in 153 Adult Patients With Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency: Analysis of the United Kingdom Congenital Adrenal Hyperplasia Adult Study Executive (CaHASE) Cohort

CONTEXT: In congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency, a strong genotype-phenotype correlation exists in childhood. However, similar data in adults are lacking. OBJECTIVE: The objective of the study was to test whether the severity of disease-causing CYP21A2 mutations inf...

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Detalles Bibliográficos
Autores principales: Krone, Nils, Rose, Ian T., Willis, Debbie S., Hodson, James, Wild, Sarah H., Doherty, Emma J., Hahner, Stefanie, Parajes, Silvia, Stimson, Roland H., Han, Thang S., Carroll, Paul V., Conway, Gerry S., Walker, Brian R., MacDonald, Fiona, Ross, Richard J., Arlt, Wiebke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2013
Materias:
JCEM Online: Advances in Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651585/
https://www.ncbi.nlm.nih.gov/pubmed/23337727
http://dx.doi.org/10.1210/jc.2012-3343

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3651585/
https://www.ncbi.nlm.nih.gov/pubmed/23337727
http://dx.doi.org/10.1210/jc.2012-3343

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