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Familial hemiplegic migraine Ca<sub>V</sub>2.1 channel mutation R192Q enhances ATP-gated P2X<sub>3 </sub>receptor activity of mouse sensory ganglion neurons mediating trigeminal pain

<p>Abstract</p> <p>Background</p> <p>The R192Q mutation of the CACNA1A gene, encoding for the α1 subunit of voltage-gated P/Q Ca<sup>2+ </sup>channels (Ca<sub>v</sub>2.1), is associated with familial hemiplegic migraine-1. We investigated whether...

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Main Authors:	Nair Asha (Author), Simonetti Manuela (Author), Birsa Nicol (Author), Ferrari Michel D (Author), van den Maagdenberg Arn MJM (Author), Giniatullin Rashid (Author), Nistri Andrea (Author), Fabbretti Elsa (Author)
Format:	Book
Published:	SAGE Publishing, 2010-08-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
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