Functional consequences of mutations in the human α(1A) calcium channel subunit linked to familial hemiplegic migraine

Journal of Neuroscience

Volumn 19, Issue 5, 1999, Pages 1610-1619

  Hans, Michael ^a   Luvisetto, Siro ^b   Williams, Mark E ^a   Spagnolo, Michele ^b   Urrutia, A ^a   Tottene, Angelita ^b   Brust, Paul F ^a   Johnson, Edwin C ^a   Harpold, Michael M ^a   Stauderman, Kenneth A ^a   Pietrobon, Daniela ^b  

^a SIBIA Corp   (United States)

^b UNIVERSITY OF PADOVA   (Italy)

Author keywords

Calcium channel; Cerebellar ataxia; Channelopathy; Familial hemiplegic migraine; Mutation; (1A) subunit

Indexed keywords

CALCIUM CHANNEL;

ANIMAL CELL; ARTICLE; CELL CULTURE; CEREBELLAR ATAXIA; FAMILIAL DISEASE; GENE EXPRESSION; GENE MUTATION; MEMBRANE CONDUCTANCE; MIGRAINE; MISSENSE MUTATION; NONHUMAN; PATCH CLAMP; PRIORITY JOURNAL;

EID: 0033103648     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.19-05-01610.1999     Document Type: Article

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