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...

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Detalhes bibliográficos
Publicado no:Pituitary
Main Authors: Elizabeth, Melitza, Hokken-Koelega, Anita C. S., Schuilwerve, Joyce, Peeters, Robin P., Visser, Theo J., de Graaff, Laura C. G.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5767207/
https://ncbi.nlm.nih.gov/pubmed/29255988
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11102-017-0850-6
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