CNRGHvan der Beek N et al. A new case of SMA phenotype without epilepsy due to biallelic variants in ASAH1 European Journal of Human Genetics 2018 27(3) doi: 10.1038/s41431-018-0250-z 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
