Szklarczyk, R., Wanschers, B. F. J., Nijtmans, L. G., Rodenburg, R. J., Zschocke, J., Dikow, N., . . . van den Heuvel, L. P. (2013). A mutation in the FAM36A gene, the human ortholog of COX20, impairs cytochrome c oxidase assembly and is associated with ataxia and muscle hypotonia. Human molecular genetics, 22(4), . https://doi.org/10.1093/hmg/dds473
Chicago Style (17th ed.) CitationSzklarczyk, Radek, et al. "A Mutation in the FAM36A Gene, the Human Ortholog of COX20, Impairs Cytochrome C Oxidase Assembly and Is Associated with Ataxia and Muscle Hypotonia." Human Molecular Genetics 22, no. 4 (2013). https://doi.org/10.1093/hmg/dds473.
MLA (9th ed.) CitationSzklarczyk, Radek, et al. "A Mutation in the FAM36A Gene, the Human Ortholog of COX20, Impairs Cytochrome C Oxidase Assembly and Is Associated with Ataxia and Muscle Hypotonia." Human Molecular Genetics, vol. 22, no. 4, 2013, https://doi.org/10.1093/hmg/dds473.