Familial hemiplegic migraine: a ion channel disorder

Brain Research Bulletin

Volumn 56, Issue 3-4, 2001, Pages 239-241

  Carrera, Paola ^a   Stenirri, Stefania ^a   Ferrari, Maurizio ^a   Battistini, Stefania ^b  

^a SAN RAFFAELE HOSPITAL   (Italy)

^b UNIVERSITY OF SIENA   (Italy)

Author keywords

CACNA1A gene; Channelopathies; Migraine; Mutations

Indexed keywords

CALCIUM CHANNEL; ION CHANNEL;

ATAXIA; CHANNEL GATING; CHROMOSOME 19P; CONFERENCE PAPER; FAMILIAL DISEASE; FAMILIAL HEMIPLEGIC MIGRAINE; GENE MUTATION; GENETIC LINKAGE; HUMAN; MIGRAINE; MISSENSE MUTATION; PRIORITY JOURNAL; TRINUCLEOTIDE REPEAT;

CALCIUM CHANNELS; HUMANS; MIGRAINE WITH AURA; MUTATION; TRINUCLEOTIDE REPEATS;

EID: 0035504920     PISSN: 03619230     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0361-9230(01)00570-6     Document Type: Conference Paper

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