Article Versions Notes

Pluta N, Hoffjan S, Zimmer F, Köhler C, Lücke T, Mohr J, Vorgerd M, Nguyen HHP, Atlan D, Wolf B, et al. Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes. 2022; 13(10):1752. https://doi.org/10.3390/genes13101752

Pluta, Natalie, Sabine Hoffjan, Frederic Zimmer, Cornelia Köhler, Thomas Lücke, Jennifer Mohr, Matthias Vorgerd, Hoa Huu Phuc Nguyen, David Atlan, Beat Wolf, and et al. 2022. "Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy" Genes 13, no. 10: 1752. https://doi.org/10.3390/genes13101752

Pluta, N., Hoffjan, S., Zimmer, F., Köhler, C., Lücke, T., Mohr, J., Vorgerd, M., Nguyen, H. H. P., Atlan, D., Wolf, B., Zaum, A.-K., & Rost, S. (2022). Homozygous Inversion on Chromosome 13 Involving SGCG Detected by Short Read Whole Genome Sequencing in a Patient Suffering from Limb-Girdle Muscular Dystrophy. Genes, 13(10), 1752. https://doi.org/10.3390/genes13101752