Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies

PURPOSE: Mutation frequencies of PROP1, POU1F1 and HESX1 in patients with combined pituitary hormone deficiencies (CPHD) vary substantially between populations. They are low in sporadic CPHD patients in Western Europe. However, most clinicians still routinely send DNA of their CPHD patients for gene...

Descripción completa

Detalles Bibliográficos
Autores principales: Elizabeth, Melitza, Hokken-Koelega, Anita C. S., Schuilwerve, Joyce, Peeters, Robin P., Visser, Theo J., de Graaff, Laura C. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767207/
https://www.ncbi.nlm.nih.gov/pubmed/29255988
http://dx.doi.org/10.1007/s11102-017-0850-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5767207/
https://www.ncbi.nlm.nih.gov/pubmed/29255988
http://dx.doi.org/10.1007/s11102-017-0850-6

Ejemplares similares