Order Article Reprints

Pegat A, Streichenberger N, Lacoste N, Hermier M, Menassa R, Coudert L, Theuriet J, Froissart R, Terrone S, Bouhour F, et al. Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report. Genes. 2022; 13(12):2245. https://doi.org/10.3390/genes13122245

Pegat, Antoine, Nathalie Streichenberger, Nicolas Lacoste, Marc Hermier, Rita Menassa, Laurent Coudert, Julian Theuriet, Roseline Froissart, Sophie Terrone, Francoise Bouhour, and et al. 2022. "Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report" Genes 13, no. 12: 2245. https://doi.org/10.3390/genes13122245

Pegat, A., Streichenberger, N., Lacoste, N., Hermier, M., Menassa, R., Coudert, L., Theuriet, J., Froissart, R., Terrone, S., Bouhour, F., Michel-Calemard, L., Schaeffer, L., & Jacquier, A. (2022). Novel Intronic Mutation in VMA21 Causing Severe Phenotype of X-Linked Myopathy with Excessive Autophagy—Case Report. Genes, 13(12), 2245. https://doi.org/10.3390/genes13122245