| PUBMED ID | 28979898 |
| DOI | 10.3389/fcvm.2017.00058 |
| TITLE | A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations |
| 2 combinations linked to 645 | OLI248; OLI249 |