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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...
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| Publicado no: | Exp Ther Med |
|---|---|
| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2019
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| Assuntos: | |
| Acesso em linha: | 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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