CNRGHGuissart C et al. Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia The American Journal of Human Genetics 2018 102(5) doi: 10.1016/j.ajhg.2018.02.021 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
