@misc{indiciae99a8985848c9,
  title = {Low frequency and rare coding variation contributes to multiple sclerosis risk},
  author = {International Multiple Sclerosis Genetics Consortium, and Mitrovic, M. and Patsopoulos, N. and Beecham, A. and Dankowski, T. and Goris, A. and Dubois, B. and Dhooghe, M.-B. and Lemmens, R. and Van Damme, P. and Fitzgerald, K. and Bach Sondergaard, H. and Sellebjerg, F. and Sorensen, P. S. and Ullum, H. and Wegner Thoerner, L. and Werge, T. and Saarela, J. and Cournu-Rebeix, I. and Damotte, V. and Fontaine, B. and Guillot-Noel, L. and Lathrop, M. and Vukusik, S. and Gourraud, P.-A. and Andlauer, T. and Pongratz, V. and Buck, D. and Gasperi, C. and Graetz, C. and Bayas, A. and Heesen, C. and Kumpfel, T. and Linker, R. and Paul, F. and Stangel, M. and Tackenberg, B. and Then Bergh, F. and Warnke, C. and Wiend},
  year = {2018},
  doi = {10.1101/286617},
  url = {https://www.biorxiv.org/content/10.1101/286617v1},
  note = {Source identifier: 10.1101/286617}
}