CNRGHProject MyocaptureLornage X et al. Novel SPEG Mutations in Congenital Myopathy without Centralized Nuclei Journal of Neuromuscular Diseases 2018 5(2) doi: 10.3233/JND-170265 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
