CNRGHYauy K et al. B3GAT3-related disorder with craniosynostosis and bone fragility due to a unique mutation Genetics in Medicine 2017 20(2) doi: 10.1038/gim.2017.109 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
