Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Mutations Within the Transcription Factor PROP1 in a Cohort of Turkish Patients with Combined Pituitary Hormone Deficiency

Objective:Mutations of the genes encoding transcription factors which play important roles in pituitary morphogenesis, differentiation and maturation may lead to combined pituitary hormone deficiency (CPHD). PROP1 gene mutations are reported as the most frequent genetic aetiology of CHPD. The aim of...

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Bibliographic Details
Main Authors: Fatma Derya Bulut, Semine Özdemir Dilek, Damla Kotan, Eda Mengen, Fatih Gürbüz, Bilgin Yüksel
Format: Article
Language:English
Published: Galenos Yayincilik 2020-09-01
Series:JCRPE
Subjects:
combined pituitary hormone deficiency
hypopituitarism
pituitary transcription factors
prop1 gene
Online Access: http://www.jcrpe.org/archives/archive-detail/article-preview/mutations-within-the-transcription-factor-iprop1-i/34597

Internet

http://www.jcrpe.org/archives/archive-detail/article-preview/mutations-within-the-transcription-factor-iprop1-i/34597

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