A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
Ben J Gu, Judith Field, Sebastien Dutertre, Amber Ou, Trevor J Kilpatrick, Jeannette Lechner-Scott, Rodney Scott, Rodney Lea, Bruce V Taylor, Jim Stankovich, Helmut Butzkueven, Melissa Gresle, Simon M Laws, Steven Petrou, Sabine Hoffjan, Denis A Akkad, Colin A Graham, Stanley Hawkins, Anna Glaser, Sahl Khalid Bedri Show all
Human Molecular Genetics | OXFORD UNIV PRESS | Published : 2015
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Awarded by National Health and Medical Research Council of Australia
This work was supported by grants from the National Health and Medical Research Council of Australia (project grants 633275, 1048082) and the Victorian Government's Operational Infrastructure Support Program.