Publication | Open Access

The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers–Danlos syndrome

Mendelian DisorderAutoimmune DiseaseGenetic DisorderMedicineGeneticsGenetic EpidemiologyPathologyVascular BiologyMolecular GeneticsDisease Gene IdentificationVariant InterpretationMolecular DiagnosticsCol3a1 Gene AssociatesVascular Ehlers–danlos Syndrome