An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor. (Q38341733)

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An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor.
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    An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor (English)

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