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

Ben J Gu; Ronald Sluyter; Kristen K Skarratt; Anne N Shemon; Lan-Phuong Dao-Ung; Stephen J Fuller; Julian A Barden; Alison L Clarke; Steven Petrou; James S Wiley

doi:10.1074/jbc.M313902200

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

Identifier:nobleid.org/w1/20260515/1ADCBF3F

Type:Journal Article

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

Identifier:nobleid.org/w1/20260515/1ADCBF3F

Type:Journal Article

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