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 o...

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Detalles Bibliográficos
Autores principales: Bulut, Fatma Derya, Özdemir Dilek, Semine, Kotan, Damla, Mengen, Eda, Gürbüz, Fatih, Yüksel, Bilgin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Galenos Publishing 2020
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499144/
https://www.ncbi.nlm.nih.gov/pubmed/31948187
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0191

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499144/
https://www.ncbi.nlm.nih.gov/pubmed/31948187
http://dx.doi.org/10.4274/jcrpe.galenos.2020.2019.0191

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