Nalaganje...
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...
Shranjeno v:
| izdano v: | Exp Ther Med |
|---|---|
| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
D.A. Spandidos
2019
|
| Teme: | |
| Online dostop: | 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 |
| Oznake: |
Označite
Brez oznak, prvi označite!
|