CNRGHBourcier R et al. Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm The American Journal of Human Genetics 2018 102(1) doi: 10.1016/j.ajhg.2017.12.006 2018 RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeToutes les publicationsGenetic diversity and differentiation among the species of African mahogany (Khaya spp.) based on a large SNP array
