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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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Detalhes bibliográficos
Main Authors: Weiner, Andrea M. J., Scampoli, Nadia L., Calcaterra, Nora B.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3266255/
https://ncbi.nlm.nih.gov/pubmed/22295061
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0029574
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