Stembalska, A.; Rydzanicz, M.; Walas, W.; Gasperowicz, P.; Pollak, A.; Pienkowski, V.M.; 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, 725.
https://doi.org/10.3390/genes13050725
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
