CNRGHMary L et al. Disease-causing variants in TCF4 are a frequent cause of intellectual disability: lessons from large-scale sequencing approaches in diagnosis European Journal of Human Genetics 2018 26(7) doi: 10.1038/s41431-018-0096-4 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
