Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome.

MLA

Varon, R., et al. “Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome.” Cell, vol. 93, no. 3, May 1998, pp. 467–76. EBSCOhost, https://doi.org/10.1016/s0092-8674(00)81174-5.

APA

Varon, R., Vissinga, C., Platzer, M., Cerosaletti, K. M., Chrzanowska, K. H., Saar, K., Beckmann, G., Seemanová, E., Cooper, P. R., Nowak, N. J., Stumm, M., Weemaes, C. M., Gatti, R. A., Wilson, R. K., Digweed, M., Rosenthal, A., Sperling, K., Concannon, P., & Reis, A. (1998). Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell, 93(3), 467–476. https://doi.org/10.1016/s0092-8674(00)81174-5

Chicago

Varon, R, C Vissinga, M Platzer, K M Cerosaletti, K H Chrzanowska, K Saar, G Beckmann, et al. 1998. “Nibrin, a Novel DNA Double-Strand Break Repair Protein, Is Mutated in Nijmegen Breakage Syndrome.” Cell 93 (3): 467–76. doi:10.1016/s0092-8674(00)81174-5.