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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Vydáno v:Front Physiol
Hlavní autoři: Cho, Kah Yan, Kelley, Brian P., Monier, Daisy, Lee, Brendan, Szabo-Rogers, Heather, Napierala, Dobrawa
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2019
Témata:
Physiology
On-line přístup: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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