Belhassen, I., Menassa, R. ., Sakka, S., Michel-Calemard, L., Streichenberger, N., Ben Ayed, D., Bouattour, N., Dammak, M. and Mhiri, C. (2023) “Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation: Novel FKRP gene mutation ”, Acta Myologica, 42(4), pp. 106–112. doi: 10.36185/2532-1900-391.