Trps1 Regulates Development of Craniofacial Skeleton and Is Required for the Initiation of Palatal Shelves Fusion

Trichorhinophalangeal syndrome (TRPS) is an autosomal dominant disorder resulting from heterozygous mutations of the TRPS1 gene. Common craniofacial abnormalities in TRPS patients include micrognathia, hypoplastic zygomatic arch, high-arched palate, and, occasionally, cleft palate. Studies have demo...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Cho, Kah Yan, Kelley, Brian P., Monier, Daisy, Lee, Brendan, Szabo-Rogers, Heather, Napierala, Dobrawa
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6509243/
https://ncbi.nlm.nih.gov/pubmed/31130868
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2019.00513
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