A novel ENG mutation causing impaired co-translational processing of endoglin associated with hereditary hemorrhagic telangiectasia
Keywords: پلی مورفیسم قطعه قطعه محدود; ALK1; activin receptor-like kinase-1; HHT; hereditary hemorrhagic telangiectasia; HHT1; HHT type 1; TGF-β, transforming growth factor-βSRP,; signal recognition particle; RFLP; restriction fragment-length polymorphism; DMEM; Dulbecco's modified Eagle's m