Fishing the Molecular Bases of Treacher Collins Syndrome

Treacher Collins syndrome (TCS) is an autosomal dominant disorder of craniofacial development, and mutations in the TCOF1 gene are responsible for over 90% of TCS cases. The knowledge about the molecular mechanisms responsible for this syndrome is relatively scant, probably due to the difficulty of...

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Detalles Bibliográficos
Autores principales: Weiner, Andrea M. J., Scampoli, Nadia L., Calcaterra, Nora B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266255/
https://www.ncbi.nlm.nih.gov/pubmed/22295061
http://dx.doi.org/10.1371/journal.pone.0029574

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3266255/
https://www.ncbi.nlm.nih.gov/pubmed/22295061
http://dx.doi.org/10.1371/journal.pone.0029574

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