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Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model

Craniosynostosis is the premature fusion of the sutures of the calvaria and is principally designated as being either syndromic (demonstrating characteristic extracranial malformations) or non-syndromic. While many forms of syndromic craniosynostosis are known to be caused by specific mutations, the...

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Detalles Bibliográficos
Autores principales: Gustafson, Jonas A., Park, Sarah S., Cunningham, Michael L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707563/
https://www.ncbi.nlm.nih.gov/pubmed/31442251
http://dx.doi.org/10.1371/journal.pone.0221402