Divergent sodium channel defects in familial hemiplegic migraine

Proceedings of the National Academy of Sciences of the United States of America

Volumn 105, Issue 28, 2008, Pages 9799-9804

  Kahlig, Kristopher M ^a   Rhodes, Thomas H ^a   Pusch, Michael ^c   Freilinger, Tobias ^d   Pereira Monteiro, José M ^e,f   Ferrari, Michel D ^g   Van Den Maagdenberg, Arn M J M ^g   Dichgans, Martin ^c   George Jr , Alfred L ^a,b  

^a VANDERBILT UNIVERSITY   (United States)

^b VANDERBILT UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c CNR   (Italy)

^d UNIVERSITY OF MUNICH   (Germany)

^e UNIVERSITY OF PORTO   (Portugal)

^f HOSPITAL DE SANTO ANTÓNIO   (Portugal)

^g LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Epilepsy; FHM3; NaV1.1; SCN1A

Indexed keywords

PROTEIN SUBUNIT; SODIUM CHANNEL;

ARTICLE; CELL SURFACE; DEPOLARIZATION; EPILEPSY; FAMILIAL HEMIPLEGIC MIGRAINE; FAMILY; GENE MUTATION; HUMAN; HUMAN CELL; INCIDENCE; PHENOTYPE; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; SODIUM CURRENT; STEADY STATE;

CELL LINE; ELECTROPHYSIOLOGY; EPILEPSY; FAMILY; HUMANS; MIGRAINE WITH AURA; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; SODIUM; SODIUM CHANNELS;

EID: 47749104145     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.0711717105     Document Type: Article

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