Associated Papers
P2X7 Variants in Pathophysiology.
Pegoraro A et al.
International Journal of Molecular Sciences, 2024
Exonic mutations in SCN9A (NaV1.7) are found in a minority of patients with erythromelalgia.
Zhang Z et al.
Scandinavian Journal of Pain, 2014
Genetics of the P2X7 receptor and human disease.
Fuller SJ et al.
Purinergic Signalling, 2009
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