CNRGHJonson PH et al. Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French families European Journal of Neurology 2018 25(5) doi: 10.1111/ene.13598 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
