An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor. (Q38341733)
Jump to navigation
Jump to search
scientific article
Language | Label | Description | Also known as |
---|---|---|---|
English | An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor. |
scientific article |
Statements
An Arg307 to Gln polymorphism within the ATP-binding site causes loss of function of the human P2X7 receptor (English)
Kristen K Skarratt
Anne N Shemon
Lan-Phuong Dao-Ung
Stephen J Fuller
Julian A Barden
Alison L Clarke
Steven Petrou