SAT-291 SIX3 Is Essential for Hypothalamic and Pituitary Development

The genetic basis for congenital hypopituitarism and related disorders is beginning to emerge, and over causal 30 genes have been identified, including six in the SHH signaling pathway. Mutations in some of these genes can also cause holoprosencephaly (HPE) or septo-optic dysplasia. SIX3 is a homeod...

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Dettagli Bibliografici
Pubblicato in:J Endocr Soc
Autori principali: Bando, Hironori, Brinkmeier, Michelle L, Castinetti, Frederic, Gergics, Peter, Mortensen, Amanda H, Ozel, Ayse Bilge, Ma, Qianyi, Li, Jun Z, Brue, Thierry, Camper, Sally A
Natura: Artigo
Lingua:Inglês
Pubblicazione: Oxford University Press 2020
Soggetti:
Neuroendocrinology and Pituitary
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207704/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.159
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