Order Article Reprints

Stembalska A, Rydzanicz M, Walas W, Gasperowicz P, Pollak A, Pienkowski VM, Biela M, Klaniewska M, Gamrot Z, Gronska E, et al. Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene. Genes. 2022; 13(5):725. https://doi.org/10.3390/genes13050725

Stembalska, Agnieszka, Małgorzata Rydzanicz, Wojciech Walas, Piotr Gasperowicz, Agnieszka Pollak, Victor Murcia Pienkowski, Mateusz Biela, Magdalena Klaniewska, Zuzanna Gamrot, Ewa Gronska, and et al. 2022. "Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene" Genes 13, no. 5: 725. https://doi.org/10.3390/genes13050725

Stembalska, A., Rydzanicz, M., Walas, W., Gasperowicz, P., Pollak, A., Pienkowski, V. M., Biela, M., Klaniewska, M., Gamrot, Z., Gronska, E., Ploski, R., & Smigiel, R. (2022). Severe Infantile Axonal Neuropathy with Respiratory Failure Caused by Novel Mutation in X-Linked LAS1L Gene. Genes, 13(5), 725. https://doi.org/10.3390/genes13050725