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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...

詳細記述

保存先:
書誌詳細
主要な著者: Weiner, Andrea M. J., Scampoli, Nadia L., Calcaterra, Nora B.
フォーマット: Artigo
言語:Inglês
出版事項: Public Library of Science 2012
主題:
オンライン・アクセス: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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