Skip to main content
Fig. 3 | Orphanet Journal of Rare Diseases

Fig. 3

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

Fig. 3

Mutations detected by whole exome sequencing. a The detailed mutation types and distribution of the mutations in the twin patients retained after filtering. b GO analysis results of all mutations retained. c The specific GOs of the twin patients compared to their parents. The GOs having similar functions with the reported pathogenesis of KC are indicated by red color. d Function prediction and sources of 12 candidate gene mutations under the polygenetic model

Back to article page