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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Detalles Bibliográficos
Autores principales: Cho, Kah Yan, Kelley, Brian P., Monier, Daisy, Lee, Brendan, Szabo-Rogers, Heather, Napierala, Dobrawa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509243/
https://www.ncbi.nlm.nih.gov/pubmed/31130868
http://dx.doi.org/10.3389/fphys.2019.00513

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509243/
https://www.ncbi.nlm.nih.gov/pubmed/31130868
http://dx.doi.org/10.3389/fphys.2019.00513

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