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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Endocr Soc
Prif Awduron: 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
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2020
Pynciau:
Neuroendocrinology and Pituitary
Mynediad Ar-lein: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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