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SLC39A5 dysfunction impairs extracellular matrix synthesis in high myopia pathogenesis

High myopia is one of the leading causes of visual impairment worldwide with high heritability. We have previously identified the genetic contribution of SLC39A5 to nonsyndromic high myopia and demonstrated that disease‐related mutations of SLC39A5 dysregulate the TGF‐β pathway. In this study, the m...

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Detalles Bibliográficos
Autores principales:	Dong, Shanshan, Tian, Qi, Zhu, Tengfei, Wang, Kangli, Lei, Ganting, Liu, Yanling, Xiong, Haofeng, Shen, Lu, Wang, Meng, Zhao, Rongjuan, Wu, Huidan, Li, Bin, Zhang, Qiumeng, Yao, Yujun, Guo, Hui, Xia, Kun, Xia, Lu, Hu, Zhengmao
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2021
Materias:	Original Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419198/ https://www.ncbi.nlm.nih.gov/pubmed/34302427 http://dx.doi.org/10.1111/jcmm.16803

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