Low frequency and rare coding variation contributes to multiple sclerosis risk
Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Harris Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie Beatrice D'hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Thorup Sellebjerg, Per Soelberg Sørensen, Henrik Ullum, Lise Wegner Thørner, Thomas Mears Werge, , Hakon H. Hakonarson
The paper identifies low-frequency coding variants contributing to multiple sclerosis risk using a large case-control study.
Cell · Oct 18, 2018Peer-reviewedGenetics