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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Bibliografske podrobnosti
izdano v: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
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2020
Teme:
Neuroendocrinology and Pituitary
Online dostop: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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