CNRGH + Projet-MyocaptureBöhm J et al. Novel ASCC1 mutations causing prenatal-onset muscle weakness with arthrogryposis and congenital bone fractures Journal of Medical Genetics 2018, vol. 56, issu 9 doi: 10.1136/jmedgenet-2018-105390 2018Grand Projet 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
