The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells.

Source:http://linkedlifedata.com/resource/pubmed/id/12527722

J. Physiol. (Lond.) 2003 Jan 15 546 Pt 2 337-47

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PMID
12527722