(Q24657270)

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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

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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 (English)
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Karim Melliti
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Manfred Grabner
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Guy R Seabrook
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15 January 2003
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546
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Pt 2
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337-47
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