Ontology highlight
ABSTRACT:
SUBMITTER: Trainor PA
PROVIDER: S-EPMC2986179 | biostudies-literature | 2009 Mar
REPOSITORIES: biostudies-literature
Trainor Paul A PA Dixon Jill J Dixon Michael J MJ
European journal of human genetics : EJHG 20081224 3
Treacher Collins syndrome (TCS) is a rare congenital disorder of craniofacial development that arises as the result of mutations in the TCOF1 gene, which encodes a nucleolar phosphoprotein known as Treacle. Individuals diagnosed with TCS frequently undergo multiple reconstructive surgeries, which are rarely fully corrective. Identifying potential avenues for rescue and/or repair of TCS depends on a profound appreciation of the etiology and pathogenesis of the syndrome. Recent research using anim ...[more]