Elicited repetitive daily blindness: A new familial disorder related to migraine and epilepsy

Neurology

Volumn 63, Issue 2, 2004, Pages 348-350

  Le Fort, Dominique ^a   Safran, A B ^b   Picard, F ^b   Bouchardy, I ^b   Morris, M A ^b  

^a Neurology Practice   (Switzerland)

^b Faculty of Medicine   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BLINDNESS; CASE REPORT; DISEASE ASSOCIATION; EPILEPSY; FAMILIAL DISEASE; HUMAN; MALE; MIGRAINE; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SYNDROME DELINEATION; VISUAL IMPAIRMENT;

EID: 3242796549     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000130251.59422.B4     Document Type: Article

References (7)

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3. De Fusco M, Marconi R, Silvestri L, et al. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump 2 subunit associated with familial hemiplegic migraine type 2. Nat Genet 2003;33:192-196.
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