Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis | Orphanet Journal of Rare Diseases | Full Text

Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis | Orphanet Journal of Rare Diseases | Full Text

Multi-level consistent changes of the ECM pathway identified in a typical keratoconus twin’s family by multi-omics analysis

Keratoconus (KC) is a common, degenerative disorder of the cornea, and genetic factors play a key role in its development. However, the genetic etiology of KC is still unclear. This study used the family of tw...

Authors:Xiao-dan Hao, Xiu-nian Chen, Yang-yang Zhang, Peng Chen, Chao Wei, Wei-yun Shi and Hua Gao

Citation:Orphanet Journal of Rare Diseases 2020 15:227

Content type:Research

 

Published on: 31 August 2020

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