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6. Functional and splicing defect analysis of 23 ACVRL1 mutations in a cohort of patients affected by Hereditary Hemorrhagic Telangiectasia. Alaa El Din F; Patri S; Thoreau V; Rodriguez-Ballesteros M; Hamade E; Bailly S; Gilbert-Dussardier B; Abou Merhi R; Kitzis A PLoS One; 2015; 10(7):e0132111. PubMed ID: 26176610 [TBL] [Abstract][Full Text] [Related]
7. BMP9 induces EphrinB2 expression in endothelial cells through an Alk1-BMPRII/ActRII-ID1/ID3-dependent pathway: implications for hereditary hemorrhagic telangiectasia type II. Kim JH; Peacock MR; George SC; Hughes CC Angiogenesis; 2012 Sep; 15(3):497-509. PubMed ID: 22622516 [TBL] [Abstract][Full Text] [Related]
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