[1]
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 (Dec. 2023), 106–112. DOI:https://doi.org/10.36185/2532-1900-391.