An Arg307 to Gln Polymorphism within the ATP-binding Site Causes Loss of Function of the Human P2X7 Receptor
Open Access
- 1 July 2004
- journal article
- Published by Elsevier
- Vol. 279 (30) , 31287-31295
- https://doi.org/10.1074/jbc.m313902200
Abstract
No abstract availableKeywords
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