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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Detalhes bibliográficos
Publicado no:J Endocr Soc
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2020
Assuntos:
Neuroendocrinology and Pituitary
Acesso em linha: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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