The molecular and cellular basis of Apert syndrome

Apert syndrome (AS) is a rare genetic and congenital disease characterized by craniosynostosis and syndactly of hands and feet. AS patients generally require lifelong management, however there are still no effective treatment methods except surgery. In recent years, research has made great progress...

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Bibliographic Details
Main Authors: Liu, Chao, Cui, Yazhou, Luan, Jing, Zhou, Xiaoyan, Han, Jinxiang
Format: Artigo
Language:Inglês
Published: International Research and Cooperation Association for Bio & Socio-Sciences Advancement 2013
Subjects:
Review
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4204555/
https://ncbi.nlm.nih.gov/pubmed/25343114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5582/irdr.2013.v2.4.115
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