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A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis
- Gu, BJ (author)
- Field, J (author)
- Dutertre, S (author)
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- Ou, A (author)
- Kilpatrick, TJ (author)
- Lechner-Scott, J (author)
- Scott, R (author)
- Lea, R (author)
- Taylor, BV (author)
- Stankovich, J (author)
- Butzkueven, H (author)
- Gresle, M (author)
- Laws, SM (author)
- Petrou, S (author)
- Hoffjan, S (author)
- Akkad, DA (author)
- Graham, CA (author)
- Hawkins, S (author)
- Matute, C (author)
- Antiguedad, A (author)
- Wiley, JS (author)
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- (creator_code:org_t)
- 2015-07-17
- 2015
- English.
- In: Human molecular genetics. - : Oxford University Press (OUP). - 1460-2083 .- 0964-6906. ; 21:14, s. NP29-NP30
- Journal article (peer-reviewed)
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- Gu, BJ
- Field, J
- Dutertre, S
- Ou, A
- Kilpatrick, TJ
- Lechner-Scott, J
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- Scott, R
- Lea, R
- Taylor, BV
- Stankovich, J
- Butzkueven, H
- Gresle, M
- Laws, SM
- Petrou, S
- Hoffjan, S
- Akkad, DA
- Graham, CA
- Hawkins, S
- Glaser, A
- Bedri, SK
- Hillert, J
- Matute, C
- Antiguedad, A
- Wiley, JS
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