Familial hemiplegic migraine type 2 is linked to 0.9Mb region on chromosome 1q23

Annals of Neurology

Volumn 53, Issue 3, 2003, Pages 376-381

  Marconi, Roberto ^a   De Fusco, Maurizio ^b   Aridon, Paolo ^b,c   Plewnia, Katrin ^a   Rossi, Maja ^a   Carapelli, Sadia ^a   Ballabio, Andrea ^d   Morgante, Letterio ^e   Musolino, Rosa ^e   Epifanio, Antonio ^e   Micieli, Giuseppe ^f   De Michele, Giuseppe ^d   Casari, Giorgio ^b  

^a MISERICORDIA HOSPITAL   (Italy)

^b SAN RAFFAELE HOSPITAL   (Italy)

^c UNIVERSITY OF PALERMO   (Italy)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^e UNIVERSITY OF MESSINA   (Italy)

^f C MONDINO NATIONAL NEUROLOGICAL INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM CHANNEL; CALSEQUESTRIN; POTASSIUM CHANNEL;

ADULT; AGED; ALPHA CHAIN; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 19; CHROMOSOME 1Q; CLINICAL ARTICLE; FAMILIAL DISEASE; FAMILIAL HEMIPLEGIC MIGRAINE; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MAPPING; GENE MUTATION; HEADACHE; HEMIPARESIS; HUMAN; MALE; MIGRAINE; PRIORITY JOURNAL; SCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; FEMALE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MIDDLE AGED; MIGRAINE WITH AURA; MUTATION; PEDIGREE;

EID: 0037371121     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10464     Document Type: Article

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