1.
Belhassen I, Menassa R, Sakka S, Michel-Calemard L, Streichenberger N, Ben Ayed D, Bouattour N, Dammak M, Mhiri C. Mild limb girdle muscular dystrophy R9 phenotype caused by novel compound heterozygous FKRP gene mutation: Novel FKRP gene mutation . Acta Myol [Internet]. 2023 Dec. 31 [cited 2024 Dec. 21];42(4):106-12. Available from: https://www.actamyologica.it/article/view/391