Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency

Background: Non-syndromic combined pituitary hormone deficiency (CPHD) occurs due to defects in transcription factors that govern early pituitary development and the specification of hormone-producing cells. The most common mutations are in the Prophet of Pit-1 (ProP1) gene. This work aims to (1) re...

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Detalles Bibliográficos
Autores principales: Moalla, Mariam, Mnif-Feki, Mouna, Safi, Wajdi, Charfi, Nadia, Mejdoub-Rekik, Nabila, Abid, Mohamed, Hadj Kacem, Faten, Hadj Kacem, Hassen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787973/
https://www.ncbi.nlm.nih.gov/pubmed/36556141
http://dx.doi.org/10.3390/jcm11247525

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9787973/
https://www.ncbi.nlm.nih.gov/pubmed/36556141
http://dx.doi.org/10.3390/jcm11247525

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