Auer-Grumbach, M., Toegel, S., Schabhüttl, M., Weinmann, D., Chiari, C., Bennett, D. H., . . . Senderek, J. (2016). Rare variants in MME, encoding metalloprotease neprilysin, are linked to late-onset autosomal-dominant axonal polyneuropathies. The American journal of human genetics, 99(3), . https://doi.org/10.1016/j.ajhg.2016.07.008
Chicago Style (17th ed.) CitationAuer-Grumbach, Michaela, et al. "Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-onset Autosomal-dominant Axonal Polyneuropathies." The American Journal of Human Genetics 99, no. 3 (2016). https://doi.org/10.1016/j.ajhg.2016.07.008.
MLA (9th ed.) CitationAuer-Grumbach, Michaela, et al. "Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-onset Autosomal-dominant Axonal Polyneuropathies." The American Journal of Human Genetics, vol. 99, no. 3, 2016, https://doi.org/10.1016/j.ajhg.2016.07.008.