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Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotype.
Cannaerts E, Kempers M, Maugeri A, Marcelis C, Gardeitchik T, Richer J, Micha D, Beauchesne L, Timmermans J, Vermeersch P, Meyten N, Chénier S, van de Beek G, Peeters N, Alaerts M, Schepers D, Van Laer L, Verstraeten A, Loeys B. Cannaerts E, et al. Among authors: vermeersch p. J Med Genet. 2019 Apr;56(4):220-227. doi: 10.1136/jmedgenet-2018-105304. Epub 2018 Jul 2. J Med Genet. 2019. PMID: 29967133
Spontaneous Coronary Artery Dissection in a Man With a Novel Missense Mutation in SMAD2 Treated by Optical Coherence Tomography-Guided Percutaneous Coronary Intervention.
Vandeloo B, Azzano A, Schoors D, Verstraeten A, Van Laer L, Loeys B, Vermeersch P. Vandeloo B, et al. Among authors: vermeersch p. JACC Cardiovasc Interv. 2019 Mar 25;12(6):e45-e47. doi: 10.1016/j.jcin.2018.09.007. Epub 2018 Nov 15. JACC Cardiovasc Interv. 2019. PMID: 30448172 Free article. No abstract available.
359 results