An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor. (Q38341733)
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Current Data About An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor.
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(P1476) "An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor" (language: en)
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(P2093) Kristen K Skarratt
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Anne N Shemon
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Lan-Phuong Dao-Ung
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Stephen J Fuller
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Julian A Barden
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Alison L Clarke
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Steven Petrou
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James S Wiley
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(P356) 10.1074/JBC.M313902200
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