Order Article Reprints

Laforgia N, De Cosmo L, Palumbo O, Ranieri C, Sesta M, Capodiferro D, Pantaleo A, Iapicca P, Lastella P, Capozza M, et al. The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein. Genes. 2020; 11(12):1519. https://doi.org/10.3390/genes11121519

Laforgia, Nicola, Lucrezia De Cosmo, Orazio Palumbo, Carlotta Ranieri, Michela Sesta, Donatella Capodiferro, Antonino Pantaleo, Pierluigi Iapicca, Patrizia Lastella, Manuela Capozza, and et al. 2020. "The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein" Genes 11, no. 12: 1519. https://doi.org/10.3390/genes11121519

Laforgia, N., De Cosmo, L., Palumbo, O., Ranieri, C., Sesta, M., Capodiferro, D., Pantaleo, A., Iapicca, P., Lastella, P., Capozza, M., Schettini, F., Bukvic, N., Bagnulo, R., & Resta, N. (2020). The First Case of Congenital Myasthenic Syndrome Caused by a Large Homozygous Deletion in the C-Terminal Region of COLQ (Collagen Like Tail Subunit of Asymmetric Acetylcholinesterase) Protein. Genes, 11(12), 1519. https://doi.org/10.3390/genes11121519