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Treacher Collins syndrome: Unmasking the role of Tcof1/treacle
Treacher Collins syndrome (TCS) is a rare congenital birth disorder characterized by severe craniofacial defects. The syndrome is associated with mutations in the TCOF1 gene which encodes a putative nucleolar phosphoprotein known as treacle. An animal model of the severe form of TCS, generated throu...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3093759/ https://ncbi.nlm.nih.gov/pubmed/19027870 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biocel.2008.10.026 |
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