Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation.

MLA

Tuppen, Helen A. L., et al. “Long-Term Survival of Neonatal Mitochondrial Complex III Deficiency Associated with a Novel BCS1L Gene Mutation.” Molecular Genetics and Metabolism, vol. 100, no. 4, Aug. 2010, pp. 345–48. EBSCOhost, https://doi.org/10.1016/j.ymgme.2010.04.010.

APA

Tuppen, H. A. L., Fehmi, J., Czermin, B., Goffrini, P., Meloni, F., Ferrero, I., He, L., Blakely, E. L., McFarland, R., Horvath, R., Turnbull, D. M., & Taylor, R. W. (2010). Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation. Molecular Genetics and Metabolism, 100(4), 345–348. https://doi.org/10.1016/j.ymgme.2010.04.010

Chicago

Tuppen, Helen A L, Janev Fehmi, Birgit Czermin, Paola Goffrini, Francesca Meloni, Iliana Ferrero, Langping He, et al. 2010. “Long-Term Survival of Neonatal Mitochondrial Complex III Deficiency Associated with a Novel BCS1L Gene Mutation.” Molecular Genetics and Metabolism 100 (4): 345–48. doi:10.1016/j.ymgme.2010.04.010.