A biallelic variant in COX18cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy

MLA

Ronchi, Dario, et al. “A Biallelic Variant in COX18cause Isolated Complex IV Deficiency Associated with Neonatal Encephalo-Cardio-Myopathy and Axonal Sensory Neuropathy.” European Journal of Human Genetics: EJHG, no. Preprints, Jan. 2023, pp. 1–7. EBSCOhost, https://doi.org/10.1038/s41431-023-01433-6.

APA

Ronchi, D., Garbellini, M., Magri, F., Menni, F., Meneri, M., Bedeschi, M. F., Dilena, R., Cecchetti, V., Picciolli, I., Furlan, F., Polimeni, V., Salani, S., Pezzoli, L., Fortunato, F., Bellini, M., Piga, D., Ripolone, M., Zanotti, S., Napoli, L., … Comi, G. P. (2023). A biallelic variant in COX18cause isolated Complex IV deficiency associated with neonatal encephalo-cardio-myopathy and axonal sensory neuropathy. European Journal of Human Genetics: EJHG, Preprints, 1–7. https://doi.org/10.1038/s41431-023-01433-6

Chicago

Ronchi, Dario, Manuela Garbellini, Francesca Magri, Francesca Menni, Megi Meneri, Maria Francesca Bedeschi, Robertino Dilena, et al. 2023. “A Biallelic Variant in COX18cause Isolated Complex IV Deficiency Associated with Neonatal Encephalo-Cardio-Myopathy and Axonal Sensory Neuropathy.” European Journal of Human Genetics: EJHG, no. Preprints (January): 1–7. doi:10.1038/s41431-023-01433-6.