Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.

MLA

Auer-Grumbach, Michaela, et al. “Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.” American Journal of Human Genetics, vol. 99, no. 3, Sept. 2016, pp. 607–23. EBSCOhost, https://doi.org/10.1016/j.ajhg.2016.07.008.

APA

Auer-Grumbach, M., Toegel, S., Schabhüttl, M., Weinmann, D., Chiari, C., Bennett, D. L. H., Beetz, C., Klein, D., Andersen, P. M., Böhme, I., Fink-Puches, R., Gonzalez, M., Harms, M. B., Motley, W., Reilly, M. M., Renner, W., Rudnik-Schöneborn, S., Schlotter-Weigel, B., Themistocleous, A. C., … Senderek, J. (2016). Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies. American Journal of Human Genetics, 99(3), 607–623. https://doi.org/10.1016/j.ajhg.2016.07.008

Chicago

Auer-Grumbach, Michaela, Stefan Toegel, Maria Schabhüttl, Daniela Weinmann, Catharina Chiari, David L H Bennett, Christian Beetz, et al. 2016. “Rare Variants in MME, Encoding Metalloprotease Neprilysin, Are Linked to Late-Onset Autosomal-Dominant Axonal Polyneuropathies.” American Journal of Human Genetics 99 (3): 607–23. doi:10.1016/j.ajhg.2016.07.008.