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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Main Authors: Fatma Derya Bulut (Author), Semine Özdemir Dilek (Author), Damla Kotan (Author), Eda Mengen (Author), Fatih Gürbüz (Author), Bilgin Yüksel (Author)
Format: Knjiga
Izdano: Galenos Yayincilik, 2020-09-01T00:00:00Z.
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