FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy

MLA

Holger Prokisch, et al. “FBXL4 Is a Mitochondria-Localized Protein in Which Autosomal Recessive Mutations Cause Multiple Respiratory Chain Multisystem Disease Commonly Involving Cortical Atrophy and Leukodystrophy.” Mitochondrion, vol. 13, Nov. 2013, pp. 939–40. EBSCOhost, https://doi.org/10.1016/j.mito.2013.07.104.

APA

Holger Prokisch, Thomas Wieland, Lee-Jun C. Wong, Emtethal Al-Jishi, Fowzan S. Alkuraya, Daniele Ghezzi, Xiaowu Gai, Claire A. Sheldon, Richard J. Rodenburg, Caroline Biagosch, Hanah Shamseldin, Tim M. Strom, Mark A. Johnson, Aurelio Reyes, Erzsebet Polyak, Satish Srinivasan, Sara Vidoni, Julian Ostrovsky, Costanza Lamperti, … Mai Tsukikawa. (2013). FBXL4 is a mitochondria-localized protein in which autosomal recessive mutations cause multiple respiratory chain multisystem disease commonly involving cortical atrophy and leukodystrophy. Mitochondrion, 13, 939–940. https://doi.org/10.1016/j.mito.2013.07.104

Chicago

Holger Prokisch, Thomas Wieland, Lee-Jun C. Wong, Emtethal Al-Jishi, Fowzan S. Alkuraya, Daniele Ghezzi, Xiaowu Gai, et al. 2013. “FBXL4 Is a Mitochondria-Localized Protein in Which Autosomal Recessive Mutations Cause Multiple Respiratory Chain Multisystem Disease Commonly Involving Cortical Atrophy and Leukodystrophy.” Mitochondrion 13 (November): 939–40. doi:10.1016/j.mito.2013.07.104.