OR16-04 OTX2 Mutations in Congenital Hypopituitarism Patients

The transcription factor OTX2 is implicated in pituitary, ocular and craniofacial development. Mutations have been described in patients with variable congenital hypopituitarism (CH) ranging from isolated growth hormone deficiency (IGHD) to combined pituitary hormone deficiency (CPHD) with/without a...

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Detalles Bibliográficos
Publicado en:J Endocr Soc
Main Authors: Gregory, Louise Cheryl, Gergics, Peter, Patti, Giuseppa, McCabe, Mark J, Maghnie, Mohamad, Spadoni, Emanuela, Camper, Sally A, Dattani, Mehul T
Formato: Artigo
Idioma:Inglês
Publicado: Oxford University Press 2020
Assuntos:
Neuroendocrinology and Pituitary
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207633/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1263
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