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PMON145 The Role of Pou3f4 in Pituitary Development and Disease

Mutations in the pituitary specific transcription factor Prophet of Pit-1 (PROP1) are the most common genetic etiology of combined pituitary hormone deficiency (CPHD), which affects 1 in 8,000 newborns worldwide. CPHD is associated with short stature, attributable to growth hormone (GH) deficiency a...

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Detalles Bibliográficos
Autores principales:	Masser, Bailey, Camper, Sally, Cheung, Leonard
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2022
Materias:	Neuroendocrinology and Pituitary
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9625297/ http://dx.doi.org/10.1210/jendso/bvac150.1124

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