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A novel mutation of FOXC1 in a Chinese family with Axenfeld-Rieger syndrome

Axenfeld-Rieger syndrome (ARS) is a disorder affecting the anterior segment of the eye and causing systemic malformations, and follows an autosomal-dominant inheritance pattern. The aim of the present study was to identify the underlying cause of ARS in a Chinese family. Genomic DNA was extracted fr...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Veröffentlicht in:Exp Ther Med
Hauptverfasser: Wu, Xing, Xie, Hai-Nan, Wu, Tong, Liu, Wei, Chen, Lan-Lam, Li, Zhao-Hui, Wang, Da-Jiang, Wang, Yi, Huang, Hou-Bin
Format: Artigo
Sprache:Inglês
Veröffentlicht: D.A. Spandidos 2019
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6676215/
https://ncbi.nlm.nih.gov/pubmed/31410177
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2019.7789
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