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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
International Research and Cooperation Association for Bio & Socio-Sciences Advancement
2013
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| Assuntos: | |
| Acesso em linha: | 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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