Novel Mutation Confirms Seizure Locus SCN1A is Also Familial Hemiplegic Migraine Locus FHM3
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference18 articles.
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2. ATP1A2: un facteur essentiel dans la migraine hémiplégique familiale;Blostein;Medecine Sciences,2006
3. Ion channel functional candidate genes in multigenic neuropsychiatric disease;Gargus;Biol Psychiatry,2006
4. Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2;De Fusco;Nat Genet,2003
5. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4;Ophoff;Cell,1996
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